Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs745542298 0.807 0.080 1 3732781 missense variant G/A;T snv 8.6E-06; 4.3E-06 2.1E-05 6
rs769809364 0.807 0.080 1 3732940 missense variant G/A snv 8.5E-06 1.4E-05 7
rs17748 0.827 0.080 11 118657714 3 prime UTR variant C/T snv 0.18 5
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs11196067 0.752 0.160 10 112709306 intron variant A/T snv 0.32 10
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205