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
rs78311289 0.662 0.357 4 1806162 missense variant A/C,G snp 4.0E-06 27
rs121913105 0.724 0.179 4 1806163 missense variant A/C,T snp 16
rs121913483 0.734 0.250 4 1801841 missense variant C/A,G,T snp 4.2E-06; 1.3E-05 3.2E-05 13
rs121913485 0.784 0.321 4 1804372 missense variant A/G snp 11
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
rs121913484 0.878 0.214 4 1804365 missense variant A/T snp 4
rs397515514 0.923 0.071 4 1807261 stop lost G/T snp 3
rs121913101 1.000 0.071 4 1807260 stop lost T/A,C,G snp 1
rs121913103 1.000 0.071 4 1807262 stop gained A/C,G,T snp 1