Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs6857 0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 16
rs769449 0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02 11
rs157582 0.851 0.160 19 44892962 intron variant C/T snv 0.24 0.29 8