Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs597808 0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs2277339 12 56752285 missense variant T/G snv 0.12 0.14 10
rs2283847
MN1
22 27785411 intron variant C/A;G;T snv 7
rs62621409 11 36437447 missense variant A/G snv 3.9E-02 3.5E-02 3
rs113931125 7 32906170 intergenic variant G/A snv 0.27 2