Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913482 0.685 0.393 4 1801837 missense variant C/T snp 30
rs121913105 0.724 0.179 4 1806163 missense variant A/C,T snp 16
rs28931614 0.744 0.179 4 1804392 missense variant G/A,C snp 11
rs28933068 0.784 0.107 4 1805644 stop gained C/A,G,T snp 1.6E-05 11
rs121913479 0.744 0.286 4 1804362 missense variant G/A,T snp 4.0E-06 3.2E-05 10
rs121913114 0.923 0.107 4 1801930 missense variant A/G,T snp 4.0E-06 2
rs75790268 0.923 0.107 4 1804377 missense variant G/T snp 2