ABO blood group predictions are brand new, and still under development. We're rolling it out to you so we can see how it performs on real data. All conclusions are still greatly limited by the general lack of phased data, the lack of genotyping at all of the necessary snps, and other factors.

best guess:

ABO blood type
A

rs8176719(D;I)
rs8176746(C;C)
rs8176747(G;G)
rs8176719(D;I) indicates you have one type-O allele
rs8176746(C;C) and rs8176747(G;G) suggests you are type-A
you were not genotyped at either rs590787 nor i4001527 so it is impossible to see your Rh blood type

But the ABO system is quite limited

Blood, you see, doesn't just come in types A, B, AB, and O. The "positive" or "negative?" Nope. In fact, let's get all the way into the weeds: Scientists have since discovered over 300 proteins that contribute to blood type. The AB+ on your blood donor card? Yeah, that's a massive oversimplification... read more at Beyond Blood Type: Genomics Can Show What You're Really Made Of

or

It would be straightforward if we all had the same blood. But we don't. On the surface of every one of our red blood cells, we have up to 342 antigens - molecules capable of triggering the production of specialised proteins called antibodies. It is the presence or absence of particular antigens that determines someone's blood type.

Some 160 of the 342 blood group antigens are 'high-prevalence', which means that they are found on the red blood cells of most people. If you lack an antigen that 99 per cent of people in the world are positive for, then your blood is considered rare. If you lack one that 99.99 per cent of people are positive for, then you have very rare blood.

If a particular high-prevalence antigen is missing from your red blood cells, then you are 'negative' for that blood group. If you receive blood from a 'positive' donor, then your own antibodies may react with the incompatible donor blood cells, triggering a further response from the immune system. These transfusion reactions can be lethal. Read more at The man with the golden blood.

Known ABO SNPs

23andMe ABO
IndexGeneSNPGenoReputeMagnitudeSummary
1   rs7466519 not tested
2 ABO rs8176750 (I;I)    
3   rs56202119 not tested
4 ABO i4000505 (G;G) Good 0
5   rs56231718 not tested
6   rs55788852 not tested
7   rs55927860 not tested
8 ABO rs8176749 (G;G)   0
9   rs56190619 not tested
10   rs55783488 not tested
11   rs56355240 not tested
12 ABO i4000504 (C;C)   0
13   rs56409303 not tested
14   rs55805279 not tested
15   rs56106480 not tested
16 ABO rs8176747 (G;G) Good 0 common in clinvar
17 ABO rs41302905 (C;C) Good 0 common in complete genomics
18 ABO rs8176746 (C;C)   0
19   rs8176745 not tested
20   rs55951833 not tested
21 ABO rs8176743 (G;G)   0
22   i5007173 not tested
23   rs55739900 not tested
24   rs56116432 not tested
25   rs56031507 not tested
26   rs8176741 not tested
27   rs56408700 not tested
28 ABO rs8176740 (T;T)   0
29   rs55827808 not tested
30   rs8176739 not tested
31   rs56223957 not tested
32   rs56189011 not tested
33   rs56089890 not tested
34   rs55727303 not tested
35 ABO rs7853989 (G;G)     Not blood group B
36   rs55964869 not tested
37   rs55756402 not tested
38   i5007171 not tested
39 ABO rs1053878 (C;C) Good 0 common in complete genomics
40   rs55658842 not tested
41   rs7873522 not tested
42   rs8176732 not tested
43 ABO rs2073824 (A;A)    
44   rs8176722 not tested
45   rs8176721 not tested
46 ABO rs8176720 (A;A)    
47 ABO rs8176719 (D;I)     most likely to be of blood type A or B
48   rs56231711 not tested
49   rs8176717 not tested
50 ABO rs512770 (G;G)    
51   rs641959 not tested
52   rs514708 not tested
53   rs55958637 not tested
54   rs549446 not tested
55 ABO rs8176704 (C;C)    
56 ABO rs574347 (T;T)    
57   rs688976 not tested
58   rs687289 not tested
59 ABO rs2073828 (A;G)    
60   rs55876802 not tested
61   rs8176694 not tested
62   rs672316 not tested
63 ABO rs657152 (G;T)    
64   rs8176682 not tested
65   rs474279 not tested
66   rs500498 not tested
67 ABO rs505922 (C;T) Bad   1.2x risk of pancreatic cancer
68 ABO rs507666 (A;G)    
69 ABO rs630014 (C;T)    
SNPedia ABO
IndexGeneSNPGenoReputeMagnitudeSummary
1 ABO rs1053878 (C;C) Good 0 common in complete genomics
2 ABO rs2073824 (A;A)    
3 ABO rs2073828 (A;G)    
4   rs2519093 not tested
5 ABO rs41302905 (C;C) Good 0 common in complete genomics
6   rs500498 not tested
7 ABO rs505922 (C;T) Bad   1.2x risk of pancreatic cancer
8 ABO rs507666 (A;G)    
9 ABO rs512770 (G;G)    
10   rs514659 not tested
11   rs55722397 not tested
12   rs55964869 not tested
13   rs56392308 not tested
14 ABO rs574347 (T;T)    
15   rs612169 not tested
16 ABO rs630014 (C;T)    
17   rs643434 not tested
18   rs644234 not tested
19 ABO rs657152 (G;T)    
20   rs687289 not tested
21   rs687621 not tested
22 ABO rs7853989 (G;G)     Not blood group B
23   rs8176694 not tested
24 ABO rs8176704 (C;C)    
25 ABO rs8176719 (D;I)     most likely to be of blood type A or B
26 ABO rs8176720 (A;A)    
27   rs8176722 not tested
28 ABO rs8176740 (T;T)   0
29   rs8176741 not tested
30 ABO rs8176743 (G;G)   0
31 ABO rs8176746 (C;C)   0
32 ABO rs8176747 (G;G) Good 0 common in clinvar
33 ABO rs8176749 (G;G)   0
34 ABO rs8176750 (I;I)    
Medicines and Drug Metabolism
Pharma
IndexGeneSNPGenoReputeMagnitudeSummary
1 ABCG2 rs2231142 (C;C) Good 0 normal
2 ABCG2 rs72552713 (G;G) Good 0 common in complete genomics
3 ANKK1 rs1800497 (C;C) Good 3 Normal (A2/A2): Better avoidance of errors. Normal OCD risk, normal Tardive Diskinesia risk, lower ADHD risk. Less Alcohol dependence. Higher risk of Postoperative Nausea. Lower obesity. Bupropion is ...
4 APOE rs429358 (T;T) Good 0 common
5 APOE rs7412 (C;C) Bad 1.1 more likely to gain weight if taking olanzapine
6 COMT rs4680 (A;A) Good 2.5 (worrier) advantage in memory and attention tasks
7 CYP1A2 rs12720461 (C;C) Good 0 normal
8   rs2069514 not tested
9   rs35694136 not tested
10 CYP1A2 rs56107638 (G;G) Good 0 common/normal
11 CYP1A2 rs762551 (A;A)   2 Fast Caffeine Metabolizer.
12   rs12721655 not tested
13 CYP2B6 rs2279343 (A;A) Good 0 common in clinvar
14 CYP2B6 rs28399499 (T;T) Good 0 common in complete genomics
15 CYP2B6 rs3211371 (C;T)    
16 CYP2B6 rs34097093 (C;C) Good 0 common in complete genomics
17 CYP2B6 rs34223104 (T;T) Good 0 common in complete genomics
18 CYP2B6 rs35303484 (A;A) Good 0 common/normal
19 CYP2B6 rs3745274 (G;G) Good 0 common in clinvar
20 CYP2C19 rs12248560 (C;C) Good 0 normal
21 CYP2C19 rs17878459 (G;G) Good 0 normal
22 CYP2C19 rs17884712 (G;G) Good 0 normal
23   rs17885098 not tested
24 CYP2C19 rs17886522 (A;A) Good 0 common/normal
25 CYP2C19 rs28399504 (A;A) Good 0 normal
26   rs3758580 not tested
27 CYP2C19 rs41291556 (T;T) Good 0 normal
28 CYP2C19 rs4244285 (G;G) Good 0 normal
29 CYP2C19 rs4986893 (G;G) Good 0 normal
30   rs55640102 not tested
31 CYP2C19 rs56337013 (C;C) Good 0 normal
32 CYP2C19 rs6413438 (C;C) Good 0 normal
33 CYP2C19 rs72552267 (G;G) Good 0 normal
34 CYP2C19 rs72558186 (T;T) Good 0 normal
35 CYP2C9 rs1057910 (A;A) Good 0.1 normal; no effect on warfarin metabolism
36 CYP2C9 rs1799853 (C;T)     CYP2C9*2 carrier; average 20% reduction in warfarin metabolism
37 CYP2C9 rs28371685 (C;C) Good 0 normal
38 CYP2C9 rs28371686 (C;C) Good 0 normal
39   rs56165452 not tested
40   rs72558187 not tested
41   rs72558188 not tested
42 CYP2C9 rs72558190 (C;C) Good 0 normal
43 CYP2C9 rs7900194 (G;G) Good 0 normal
44 CYP2C9 rs7900194 (G;G) Good 0 normal
45 CYP2C9 rs9332130 (A;A) Good 0 normal
46 CYP2C9 rs9332131 (I;I)     normal
47 CYP2C9 rs9332239 (C;C) Good 0 normal
48 CYP2D6 rs1065852 (C;C) Good 0 normal
49   rs1080985 not tested
50   rs147960066 not tested
51 CYP2D6 rs16947 (A;A) Good 0 Homozygous for CYP2D6 variants (non-CYP2D6*1)
52 CYP2D6 rs28371706 (C;T)     Carrier of one CYP2D6 variant, possibly decreased on non-functioning.
53   rs28371720 not tested
54 CYP2D6 rs28371725 (G;G) Good 0 normal
55 CYP2D6 rs35742686 (I;I)    
56 CYP2D6 rs3892097 (G;G) Good 0 extensive metabolizer
57 CYP2D6 rs5030655 (I;I)     normal
58   rs5030862 not tested
59   rs5030863 not tested
60 CYP2D6 rs5030865 (C;C) Good 1 normal
61 CYP2D6 rs5030865 (C;C) Good 1 normal
62 CYP2D6 rs5030867 (A;A) Good 0 normal
63 CYP2D6 rs59421388 (C;C) Good 0 common in complete genomics
64   rs72549349 not tested
65   rs72549351 not tested
66   rs72549353 not tested
67   rs72549354 not tested
68   rs72549357 not tested
69   rs769258 not tested
70   rs12721629 not tested
71 CYP3A rs2740574 (A;A) Good 0 normal
72   rs35599367 not tested
73 CYP3A4 rs4646438 (D;D)    
74 CYP3A4 rs4986910 (T;T) Good 0 normal
75 CYP3A4 rs4987161 (T;T) Good 0 normal
76 CYP3A4 rs55785340 (A;A) Good 0 normal
77 CYP3A5 rs10264272 (C;C) Good 0 normal
78   rs15524 not tested
79 CYP3A5 rs28365083 (C;C) Good 0 normal
80 CYP3A5 rs28383468 (C;C) Good 0 normal
81 CYP3A5 rs28383479 (G;G) Good 0 normal
82 CYP3A5 rs41279854 (A;A) Good 0 normal
83 CYP3A5 rs41303343 (I;I)     CYP3A5*7 homozygote; nonexpressor for CYP3A5
84 CYP3A5 rs55817950 (G;G) Good 0 normal
85   rs55965422 not tested
86 CYP3A5 rs776746 (G;G) Bad 2.5 CYP3A5*3 homozygote; CYP3A5 non-expressor
87   rs1799963 not tested
88 F5 rs6025 (G;G) Good 0 normal/common
89 MTHFR rs1801131 (A;C) Bad 2.1 Possibly impaired folate metabolism
90 MTHFR rs1801133 (C;T) Bad 2.2 1 copy of C677T allele of MTHFR = 65% efficiency in processing folic acid
91 OPRM1 rs1799971 (A;A) Good 0 normal
92 SLCO1B1 rs2306283 (C;T)    
93 SLCO1B1 rs4149056 (C;T) Bad 2.1 reduced breakdown of some drugs; 5x increased myopathy risk for statin users
94   rs55737008 not tested
95 SLCO1B1 rs56061388 (T;T)    
96   rs56101265 not tested
97   rs59502379 not tested
98   rs72559745 not tested
99 UGT2B15 rs1902023 (G;G)    
100 VKORC1 rs8050894 (C;G)     average warfarin response (~5 mg/day)
101 VKORC1 rs9923231 (C;T)   2 reduced warfarin dose if treated for VTE
102 VKORC1 rs9934438 (A;G)