Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs17561 0.672 0.560 2 112779646 missense variant C/A snv 0.27 0.26 23
rs396991 0.742 0.480 1 161544752 missense variant A/C;G;T snv 0.33; 4.1E-06 14