Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5985
F13A1
0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 20
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv 15
rs1063856
VWF
0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 14
rs1410996
CFH
0.807 0.240 1 196727803 intron variant G/A snv 0.46 11
rs8176749
ABO
1.000 0.040 9 133255801 synonymous variant C/T snv 0.12 0.11 7
rs8176704
ABO
0.925 0.080 9 133260148 intron variant G/A snv 5
rs4915559
CFHR4 ; LOC105371675
1.000 0.040 1 196917640 intron variant T/A;C snv 4
rs1063857
VWF
12 6044348 synonymous variant A/G snv 0.31 0.40 4
rs12116643
CFHR5
1 197004053 intron variant T/C snv 0.19 3
rs11243081 6 6337273 intergenic variant C/T snv 0.23 2
rs1318606 6 6331703 intergenic variant T/C snv 0.38 2
rs17142067 6 6341054 intergenic variant A/C;G snv 0.23 2
rs4686760 3 184796825 intergenic variant G/A;C snv 2
rs555212 13 113102226 upstream gene variant A/G snv 0.79 2
rs9533425 13 43196338 regulatory region variant G/C snv 0.14 2
rs10922162
ASPM
1 197101646 synonymous variant C/T snv 0.26 0.16 2
rs379440
EPB41L4A
5 112357674 intron variant T/C snv 3.5E-02 2
rs3211770
F10
13 113139535 intron variant G/A snv 0.11 2
rs3024321
F13A1
6 6317893 intron variant A/G snv 0.29 2
rs6041
F7
13 113118393 intron variant G/A snv 0.13 0.12 2
rs6708166
LBH
2 30303914 intron variant G/A snv 0.32 2
rs2022309
LOC105378861
1 94586920 intron variant G/T snv 0.23 2
rs10665
MCF2L
13 113098517 3 prime UTR variant A/G snv 0.12 2
rs2181540
MCF2L
13 113098850 3 prime UTR variant T/C snv 0.15 2
rs10982156
ORM1
9 114325784 intron variant T/A snv 7.0E-02 2