Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2963472 5 158572014 intron variant G/A;C snv 3
rs4475251 5 115039988 intergenic variant G/A;T snv 3
rs453301 8 9172877 intron variant T/G snv 0.54 3
rs4767293 12 112025492 downstream gene variant A/G snv 0.53 3
rs58084604 18 60182196 intergenic variant C/T snv 0.24 3
rs73029563 2 164151656 intron variant C/G;T snv 3
rs7446877 5 158441123 intron variant C/G;T snv 3
rs871606 4 53933078 intron variant T/C;G snv 3
rs9375463 6 126845743 intron variant A/C;T snv 3
rs9491694 6 127115955 intron variant T/A snv 0.30 3
rs10092965 8 8515975 intergenic variant A/G snv 0.43 2
rs10503387 8 9293015 intron variant C/T snv 0.33 2
rs10741534 11 11233360 intergenic variant T/A;C snv 2
rs10955992 8 120860224 intergenic variant A/C;T snv 2
rs1111336 2 28435029 regulatory region variant A/C;G snv 2
rs11246533 11 54742025 intergenic variant G/A snv 0.11 2
rs11756347 6 126856325 intron variant A/G snv 0.36 2
rs11781008 8 9295729 intron variant G/C;T snv 2
rs1214759 6 43385242 intron variant A/G snv 0.56 2
rs12194642 6 78829074 intergenic variant G/A snv 0.32 2
rs13225723 7 106776021 splice region variant G/A snv 0.19 2
rs13249843 8 11601509 regulatory region variant G/T snv 0.32 2
rs13270194 8 8520592 regulatory region variant T/C snv 0.58 2
rs1584063 3 12225355 intergenic variant G/A snv 0.51 2
rs17083718 4 53935382 intron variant A/G snv 0.12 2