Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47
rs375874539 0.732 0.320 17 7674237 missense variant G/A;C snv 15
rs3761548 0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs438034 0.882 0.120 1 214657274 stop gained A/G;T snv 0.61 4
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4987188 0.790 0.200 2 47416318 missense variant G/A;T snv 1.3E-02; 2.0E-05 11
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs9282861 0.658 0.440 16 28606193 missense variant C/T snv 31