Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10249276 7 118938630 intergenic variant A/G;T snv 1
rs10281955 7 118944637 intergenic variant G/A snv 0.86 1
rs10433415 3 133566686 intergenic variant G/T snv 0.57 1
rs10935068 3 133543963 upstream gene variant T/A;G snv 1
rs10953881 7 118968071 intergenic variant C/G;T snv 1
rs10953885 7 118968349 intergenic variant T/A;C snv 1
rs11128951 3 20334054 intron variant A/G snv 0.19 1
rs115888294 8 94105161 upstream gene variant T/C snv 2.4E-02 1
rs11766519 7 57524150 intergenic variant T/C snv 0.13 1
rs12108602 4 114719413 upstream gene variant A/G snv 0.18 1
rs12292796 11 39404549 intergenic variant A/C snv 0.10 1
rs13250871 8 11610254 intergenic variant G/A snv 0.28 1
rs1371187 2 164188591 intron variant A/G snv 0.52 1
rs139077481 11 107579224 intergenic variant T/C snv 3.2E-03 1
rs140520944 18 29508647 intergenic variant G/T snv 4.7E-03 1
rs142673685 19 31669942 intergenic variant C/T snv 4.0E-03 1
rs1444600 3 133569662 upstream gene variant C/T snv 0.57 1
rs170099 7 119360158 intergenic variant C/T snv 0.84 1
rs17144687 5 118824240 intergenic variant A/C snv 4.5E-02 1
rs2244894 8 11591150 intergenic variant G/C snv 0.45 1
rs2677485 2 155678644 intergenic variant T/A;C snv 1
rs2749097 1 63661797 downstream gene variant C/G snv 0.19 1
rs3860498 3 133541672 downstream gene variant T/A;C snv 1
rs4017074 3 133541583 downstream gene variant T/C snv 0.71 1
rs4268066 7 118961051 intergenic variant C/T snv 0.86 1