Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1052667 0.882 0.040 19 47004177 3 prime UTR variant C/G;T snv 6
rs1136201 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121912664 0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 44
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104