Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10220265 13 103397233 downstream gene variant G/A snv 0.28 1
rs10792320 11 61978819 intergenic variant A/C;T snv 1
rs10897208 11 62024415 intergenic variant A/T snv 0.11 1
rs11230874 11 62028114 intergenic variant T/G snv 6.9E-02 1
rs1145652 5 165337081 intergenic variant A/G snv 9.6E-02 1
rs12423247 12 96464584 intron variant A/T snv 9.2E-02 1
rs12459897 19 31105872 intron variant G/T snv 1.2E-02 1
rs12526913 6 11082691 downstream gene variant A/G;T snv 1
rs12587311 14 28647489 intergenic variant T/C snv 0.53 1
rs12665478 6 11080592 downstream gene variant G/A snv 0.41 1
rs1330767 13 103408241 intergenic variant C/T snv 0.21 1
rs1424760 2 162925277 intergenic variant C/T snv 0.52 1
rs1692120 11 61650000 downstream gene variant G/A snv 0.43 1
rs174627 11 61869994 downstream gene variant G/A snv 0.10 1
rs2028062 11 61978481 intergenic variant G/A;C snv 1
rs2210152 13 103409236 intergenic variant T/C snv 0.22 1
rs2210153 13 103409291 intergenic variant G/A snv 0.22 1
rs2585617 6 68627895 non coding transcript exon variant A/G snv 0.90 1
rs3845427 1 181293302 intergenic variant T/A snv 0.52 1
rs4713169 6 11084321 intergenic variant G/C snv 0.45 1
rs4963444 11 62005870 regulatory region variant G/A;T snv 1
rs7490068 13 103408045 intergenic variant G/A;C snv 1
rs8012543 14 28618344 upstream gene variant G/A snv 0.50 1
rs9437689 1 95083980 regulatory region variant C/T snv 0.34 1
rs9586177 13 103407580 intergenic variant C/T snv 0.21 1