Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs153109 0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs17855750 0.695 0.480 16 28503907 missense variant A/C;T snv 6.4E-02; 4.0E-06 21