Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1927914
TLR4
0.732 0.520 9 117702447 upstream gene variant G/A snv 0.52 14
rs12778366
SIRT1
0.724 0.480 10 67883321 upstream gene variant T/C;G snv 13
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 13
rs2146323
VEGFA
0.752 0.480 6 43777358 non coding transcript exon variant C/A snv 0.31 13
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 12
rs1063320
HLA-G
0.752 0.360 6 29830972 3 prime UTR variant C/G;T snv 12
rs12153855
TNXB
0.776 0.320 6 32107027 intron variant T/C snv 0.11 11
rs137853006
PROM1
0.776 0.080 4 16013299 missense variant G/A snv 11
rs1410996
CFH
0.807 0.240 1 196727803 intron variant G/A snv 0.46 11
rs61755783
PRPH2
0.763 0.080 6 42721911 missense variant G/A snv 1.4E-05 11
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 10
rs1864163
CETP
0.882 0.120 16 56963321 intron variant G/A snv 0.26 10
rs2269426
TNXB
0.807 0.280 6 32108722 intron variant G/A snv 0.35 10
rs28366003
MT2A
0.763 0.240 16 56608579 upstream gene variant A/C;G snv 4.6E-02 10
rs61755792
PRPH2
0.763 0.160 6 42721821 missense variant G/A;C snv 10
rs10737680
CFH
0.827 0.080 1 196710325 intron variant A/C snv 0.44 9
rs1329428
CFH
0.807 0.160 1 196733680 intron variant C/T snv 0.44 9
rs2043085
ALDH1A2
0.827 0.080 15 58388755 intron variant T/C snv 0.54 9
rs2740488
ABCA1
0.827 0.120 9 104899461 intron variant A/C snv 0.29 9
rs3093077 0.827 0.200 1 159709846 upstream gene variant A/C;G;T snv 9
rs57137919
ABCG1 ; LOC105372814
0.776 0.160 21 42218908 intron variant G/A snv 0.14 9
rs13278062
LOC389641 ; TNFRSF10A
0.807 0.200 8 23225458 non coding transcript exon variant G/A;C;T snv 8
rs243866
MMP2
0.827 0.120 16 55477625 intron variant G/A snv 0.19 8
rs3793784
ERCC6
0.827 0.120 10 49539493 5 prime UTR variant G/C snv 0.30 8
rs9582036
FLT1
0.776 0.280 13 28311271 intron variant C/A snv 0.59 8