Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121434592 0.582 0.500 14 104780214 missense variant C/T snp 4.0E-06 25
rs113488022 0.407 0.786 7 140753336 missense variant snp 4.0E-06 21
rs138213197 0.744 0.179 17 48728343 missense variant C/T snp 1.8E-03 2.2E-03 3
rs121913430 1.000 0.071 7 55174740 missense variant G/A snp 2
rs182052 0.801 0.250 3 186842993 intron variant G/A snp 0.39 1
rs17366568 3 186852664 non coding transcript exon variant G/A snp 8.8E-02 1
rs137852578
AR
0.878 0.071 X 67723710 missense variant A/G snp 1
rs137852581
AR
0.923 0.071 X 67723701 missense variant C/T snp 1
rs339331 0.878 0.071 6 116888889 intron variant T/C snp 0.30 1