Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs851023 0.925 0.080 6 36038443 intron variant G/A snv 0.89 2
rs12199654 1.000 0.080 6 36041718 intron variant A/G snv 4.2E-02 1
rs3804452 1.000 0.040 6 36109157 3 prime UTR variant G/A snv 8.6E-02 1
rs7761118 1.000 0.040 6 36100526 intron variant G/A snv 0.14 1
rs780319980 1.000 0.080 6 36102610 missense variant A/G snv 1.2E-05 1