Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs61194703 19 11081517 downstream gene variant A/T snv 0.14 2
rs6141803 1.000 0.120 20 32752550 TF binding site variant T/C snv 0.13 2
rs62052820 16 69541335 intergenic variant G/A snv 0.17 2
rs6684311 1.000 0.120 1 166516654 intergenic variant C/G snv 0.22 2
rs6686889 1 24703979 upstream gene variant C/A;G;T snv 2
rs6819003 4 38357696 intergenic variant G/A snv 0.59 2
rs708494 1.000 0.040 14 52300623 regulatory region variant G/A snv 0.47 2
rs876538 1 159705927 upstream gene variant T/A;C snv 2
rs943580 1 230701298 upstream gene variant G/A snv 0.42 2
rs9506725 13 21740007 regulatory region variant T/C snv 0.30 2
rs10042590 5 88477501 intron variant G/A snv 5.8E-02 1
rs10850407 12 114940232 intergenic variant T/G snv 0.24 1
rs113602013 18 60252477 intergenic variant G/A;C snv 1
rs1149643 1 56163763 intron variant A/T snv 0.49 1
rs11605518 11 13248667 intergenic variant A/G snv 0.72 1
rs11826048 11 103527569 intergenic variant C/T snv 9.6E-02 1
rs12324159 15 41170270 regulatory region variant G/A snv 0.47 1
rs12358504 10 121240352 intergenic variant A/G snv 0.18 1
rs13021222 2 164191395 intron variant G/C;T snv 1
rs13265769 8 81912028 intron variant T/C snv 0.35 1
rs13358657 5 158511062 intron variant A/G snv 0.11 1
rs142076278 16 51794418 intergenic variant A/G snv 9.5E-03 1
rs150532297 5 158169198 downstream gene variant G/A snv 4.1E-03 1
rs1507151 6 78773529 intergenic variant T/C snv 0.32 1
rs17006217 3 19741785 intergenic variant T/A;C snv 1