Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs137852564
AR
0.827 0.240 X 67722976 missense variant G/A;T snv 3
rs55770810 0.763 0.280 17 43063931 missense variant G/A;T snv 2.4E-05; 8.0E-06 3
rs80357474 0.827 0.200 17 43049188 missense variant A/C;G;T snv 8.0E-06 3
rs121964872 0.882 0.120 16 68833362 missense variant A/G snv 4.4E-05 1.1E-04 3
rs121913413 0.763 0.240 3 41224634 missense variant C/A;T snv 3
rs121913403 0.683 0.240 3 41224622 missense variant C/A;G;T snv 3
rs61753793 0.851 0.120 2 47799002 missense variant T/C snv 3.6E-05 5.6E-05 3
rs776587763 0.790 0.120 10 121520085 missense variant C/A;T snv 4.0E-06; 4.0E-06 3
rs121918502 0.790 0.160 10 121517351 missense variant G/C snv 3
rs28936683 0.882 0.080 20 35434093 missense variant A/G snv 7.0E-06 3
rs121909352 0.882 0.120 8 96145185 missense variant G/T snv 2.0E-03 2.0E-03 3
rs36119840 0.807 0.280 5 37816010 missense variant G/A snv 2.3E-03 2.7E-03 3
rs192732174 0.827 0.160 3 33068245 missense variant G/A;T snv 4.0E-05; 3.6E-05 3
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 3
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 3
rs57520892 0.776 0.200 1 156137204 missense variant G/A;C snv 4.1E-05 3
rs60890628 0.776 0.200 1 156138507 missense variant C/T snv 1.5E-04 1.0E-04 3
rs121908670 0.882 0.080 11 68363784 missense variant G/A snv 3
rs28940291 0.776 0.080 1 11992660 missense variant G/A snv 4.0E-06 3
rs281865127
MPZ
0.827 0.120 1 161306767 missense variant T/C snv 3
rs63750664 0.882 0.200 2 47783292 missense variant C/A;T snv 4.1E-06; 9.4E-05 3
rs2020912 0.807 0.480 2 47800616 missense variant T/C;G snv 5.1E-03 3
rs104894119 0.807 0.160 9 124500685 missense variant C/T snv 3
rs121913272 0.752 0.400 3 179210192 missense variant T/C;G snv 3
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 3