Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs587780073 0.708 0.400 17 7674262 missense variant T/C;G snv 17
rs869025608 0.763 0.400 15 66435117 missense variant G/C;T snv 9
rs1057519977 0.763 0.360 17 7675189 missense variant G/C snv 13
rs1057519978 0.763 0.360 17 7675191 missense variant A/C;G;T snv 12
rs121912666 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 24
rs587778720 0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 25
rs1057519932 0.683 0.320 3 179234298 missense variant T/G snv 22
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 28
rs121913275 0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 25
rs786202962 0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06 17
rs864622237 0.716 0.320 17 7674263 missense variant A/C;G;T snv 17
rs1057519883 0.742 0.280 9 21971120 missense variant C/G;T snv 11
rs1057519946 0.732 0.280 19 52212729 missense variant C/G;T snv 17
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 20
rs530941076 0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 20
rs587777790 0.732 0.280 3 179199690 missense variant G/A snv 12
rs587782329 0.677 0.280 17 7674217 missense variant C/A;G;T snv 16
rs1057519909 0.790 0.240 15 66435116 missense variant A/C snv 6
rs1057519927 0.716 0.240 3 179218295 missense variant A/C;G;T snv 18
rs397517201 0.732 0.240 3 179218307 missense variant A/C;G;T snv 14
rs587782289 0.752 0.240 17 7674257 missense variant A/C;G;T snv 12
rs967461896 0.724 0.240 17 7675086 missense variant A/C;G;T snv 16
rs1057519940 0.752 0.200 3 179218308 missense variant G/T snv 13
rs1057519938 0.776 0.160 3 179203764 missense variant A/C;T snv 10
rs1057519939 0.776 0.160 3 179203763 missense variant A/C snv 10