Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1003643 1.000 0.080 22 39280489 downstream gene variant T/G snv 0.34 1
rs1003644 1.000 0.080 22 39280739 downstream gene variant G/A snv 0.31 1
rs1005999 1.000 0.080 2 104907333 intron variant C/T snv 0.25 1
rs1008591 1.000 0.080 19 46227357 upstream gene variant A/G snv 0.45 1
rs1019212 1.000 0.080 19 46225962 upstream gene variant G/A snv 0.45 1
rs10607450 1.000 0.080 11 118812058 regulatory region variant T/C snv 0.19 1
rs10892294 1.000 0.080 11 118796648 downstream gene variant G/C snv 0.19 1
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 1
rs11117432 0.851 0.200 16 85985665 upstream gene variant G/A snv 0.15 1
rs11117433 0.827 0.160 16 85985910 upstream gene variant G/A;C;T snv 1
rs111413387 1.000 0.080 17 46267043 non coding transcript exon variant A/C snv 0.14 1
rs11237982 1.000 0.080 11 79730650 intergenic variant T/C snv 0.18 1
rs1158810 1.000 0.080 9 119047241 intergenic variant T/C snv 0.50 1
rs11604811 1.000 0.080 11 72678939 upstream gene variant G/A;T snv 1
rs11655972 1.000 0.080 17 39250819 downstream gene variant C/T snv 0.78 1
rs11724614 1.000 0.080 4 102629091 downstream gene variant A/G snv 0.55 1
rs12103884 1.000 0.080 17 39889472 intergenic variant C/T snv 0.45 1
rs12134279 0.925 0.080 1 197812068 regulatory region variant C/T snv 0.17 1
rs12358982 1.000 0.080 10 104094571 regulatory region variant A/G snv 0.14 1
rs12437560 1.000 0.080 15 61832507 upstream gene variant T/G snv 0.20 1
rs12453507 0.925 0.200 17 39896954 intergenic variant C/G;T snv 1
rs12627970 1.000 0.080 22 39325740 TF binding site variant A/G snv 0.19 1
rs12694574 1.000 0.080 2 222129014 intergenic variant T/C snv 0.16 1
rs12939565 1.000 0.080 17 39882136 downstream gene variant A/T snv 0.41 1
rs12941333 1.000 0.080 17 39884281 intergenic variant C/T snv 0.39 1