Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs12203592 0.649 0.320 6 396321 intron variant C/T snv 0.10 38
rs1126809 0.683 0.320 11 89284793 missense variant G/A snv 0.18 0.18 29
rs1805007 0.695 0.280 16 89919709 missense variant C/A;G;T snv 4.4E-02 25
rs1800407 0.807 0.200 15 27985172 missense variant C/T snv 4.7E-02 4.9E-02 10