Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs116843064 0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 16
rs198851 6 26104404 downstream gene variant T/A;C;G snv 15
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 15
rs112259268 17 43797377 downstream gene variant C/A snv 1.9E-02 6
rs62434129 6 150687701 intron variant A/G;T snv 8.8E-02 6
rs1799852
TF
3 133756878 synonymous variant C/T snv 0.13 0.11 5
rs7140110 13 113841051 non coding transcript exon variant T/C snv 0.28 4