Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16969968 0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 4
rs684513 0.925 0.080 15 78566058 intron variant C/G;T snv 3
rs2629540 0.925 0.080 10 124737579 intron variant G/C snv 0.18 3
rs111325002 1.000 0.080 3 96134788 intergenic variant A/G snv 8.6E-03 2
rs150954431 1.000 0.080 12 124517777 intron variant C/T snv 1.6E-02 2
rs2005290 1.000 0.080 17 3284718 intron variant C/G;T snv 2
rs12071360 1.000 0.080 1 233608833 intergenic variant T/C snv 0.10 1
rs13273442 0.882 0.080 8 42688874 intergenic variant A/G snv 0.66 1