Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10055396 5 148182067 intron variant A/G;T snv 1
rs1005636 19 43302407 downstream gene variant T/C snv 0.88 1
rs10139058 14 106685899 upstream gene variant C/T snv 0.42 1
rs10144381 14 100706960 regulatory region variant C/A;G;T snv 1
rs10179654 2 102305323 regulatory region variant T/G snv 0.55 1
rs1019016 7 80941246 regulatory region variant G/T snv 0.53 1
rs10262428 7 80940826 TF binding site variant T/G snv 0.37 1
rs10425544 19 836043 upstream gene variant T/C snv 0.79 1
rs10447396 6 36145821 downstream gene variant G/A snv 0.25 1
rs10502249 11 122633543 regulatory region variant G/A;T snv 1
rs10690148 11 18271957 downstream gene variant -/ACTTA delins 0.82 1
rs10762489 10 71891700 intergenic variant A/G snv 0.30 1
rs10781540 9 136427384 downstream gene variant G/A snv 0.42 1
rs10794181 10 124284185 intergenic variant G/A;C snv 1
rs10852587 16 48972547 intergenic variant T/A snv 0.23 1
rs10903002 16 1274458 intron variant G/C snv 0.58 1
rs1092801 1 196759905 intergenic variant G/C;T snv 1
rs10931256 2 186820468 intergenic variant T/C snv 0.20 1
rs10933394 2 232384370 upstream gene variant T/A;C snv 1
rs10935473 3 98698056 intergenic variant G/T snv 0.36 1
rs10972076 9 34356361 regulatory region variant C/T snv 0.47 1
rs10972159 9 34593088 upstream gene variant G/A snv 4.1E-02 1
rs1097234 1 52597887 upstream gene variant C/A snv 0.12 1
rs11003118 10 52759390 upstream gene variant T/C snv 0.28 1
rs11006489 10 46049486 upstream gene variant C/G;T snv 1