Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs67150165 1 169494279 non coding transcript exon variant A/-;AA delins 1
rs641959
ABO
9 133258308 intron variant A/C snv 0.29 4
rs16861990
NME7
1 169165889 intron variant A/C snv 5.5E-02 2
rs4572916
F11-AS1
4 186302429 intron variant A/C snv 0.22 2
rs6687813 1 169508336 downstream gene variant A/C snv 0.93 2
rs12554339
ABO
9 133253350 non coding transcript exon variant A/C snv 0.25 1
rs557317 9 133281464 intergenic variant A/C snv 0.30 1
rs4613610
F11-AS1
4 186301117 intron variant A/C;G snv 1
rs492488
ABO
9 133269548 intron variant A/C;G;T snv 3
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 22
rs6427195
F5
1 169511938 downstream gene variant A/C;T snv 2
rs10800427
NME7
1 169303213 non coding transcript exon variant A/C;T snv 0.96 1
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv 15
rs507666
ABO
1.000 0.040 9 133273983 intron variant A/G snv 8
rs641943
ABO
9 133258323 intron variant A/G snv 0.29 4
rs1018827
F5
1 169544768 intron variant A/G snv 0.92 2
rs10737547 1 169506814 intergenic variant A/G snv 0.93 2
rs2420372
F5
1 169528818 intron variant A/G snv 0.95 2
rs3756009
F11
4 186264957 upstream gene variant A/G snv 0.32 2
rs6696217 1 169491488 non coding transcript exon variant A/G snv 0.92 2
rs7857390
ABO
9 133253159 non coding transcript exon variant A/G snv 0.67 2
rs10800448 1 169491168 non coding transcript exon variant A/G snv 0.72 1
rs11244053
ABO
9 133253973 non coding transcript exon variant A/G snv 0.27 1
rs117134629 9 133304245 downstream gene variant A/G snv 7.5E-02 1
rs12554336
ABO
9 133253276 non coding transcript exon variant A/G snv 0.27 1