Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 10
rs10885122 1.000 0.080 10 111282335 intergenic variant T/G snv 0.71 4
rs11257655 1.000 0.080 10 12265895 TF binding site variant C/T snv 0.23 4
rs13023194 0.925 0.120 2 27744393 intergenic variant G/A;C snv 4
rs1483121 1.000 0.080 11 48311808 downstream gene variant G/A snv 9.7E-02 4
rs2191349 1.000 0.080 7 15024684 intergenic variant G/T snv 0.54 4
rs4502156 1.000 0.080 15 62090956 intergenic variant T/C snv 0.55 4
rs10228456 1.000 0.080 7 15024301 intergenic variant C/T snv 0.54 3
rs12440695 15 62142957 regulatory region variant T/C snv 0.32 3
rs576674 1.000 0.080 13 32980164 intergenic variant G/A snv 0.69 3
rs10747083 12 132465032 downstream gene variant G/A;T snv 2
rs11039130 11 47207765 intergenic variant C/T snv 0.20 2
rs11195502 10 111279909 intergenic variant C/A;G;T snv 2
rs11607883 11 45818158 intron variant G/A snv 0.40 2
rs11782386 8 9344277 intron variant C/T snv 9.7E-02 2
rs118137427 10 111217250 intergenic variant A/G snv 3.3E-02 2
rs1280 3 170995501 intron variant T/C snv 0.20 2
rs4775471 15 62132450 intergenic variant C/T snv 0.18 2
rs983309 8 9320222 intron variant T/G snv 0.82 2
rs853789
ABCB11
2 168944978 intron variant A/G;T snv 0.75 4
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 9
rs2877716
ADCY5
3 123375604 intron variant T/C snv 0.76 4
rs11717195
ADCY5
1.000 0.080 3 123363551 intron variant T/C snv 0.19 3
rs11715915
AMT
3 49417897 synonymous variant C/A;T snv 0.28 2