Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1057519947 0.790 0.160 19 52212730 missense variant G/A snv 9
rs1057519999 0.763 0.160 17 7674247 missense variant T/C;G snv 12
rs121913284 0.776 0.160 3 179203765 missense variant T/A;G snv 10
rs876660807 0.763 0.160 17 7674248 missense variant T/C snv 12
rs1057519912 0.776 0.200 X 71129408 missense variant C/G;T snv 5
rs1057519940 0.752 0.200 3 179218308 missense variant G/T snv 13
rs1057520009 0.790 0.200 2 61492337 missense variant C/T snv 4.4E-06 5
rs1057520010 0.882 0.200 2 61492336 missense variant T/A;G snv 5
rs1057519927 0.716 0.240 3 179218295 missense variant A/C;G;T snv 18
rs1057520006 0.752 0.240 17 7673799 missense variant A/C;G;T snv 12
rs397517201 0.732 0.240 3 179218307 missense variant A/C;G;T snv 14
rs587781991 0.724 0.240 17 7675208 missense variant C/A;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
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
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