Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs1884444 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 34
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs6679677 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 26
rs768623239 0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05 26
rs35829419 0.689 0.560 1 247425556 missense variant C/A snv 3.9E-02 3.3E-02 23
rs35761398 0.701 0.520 1 23875429 missense variant TT/CC mnv 19
rs7517847 0.689 0.600 1 67215986 intron variant T/G snv 0.37 19
rs2501432 0.716 0.480 1 23875430 missense variant T/C;G snv 0.62 16
rs367543041 0.742 0.200 1 11022553 missense variant G/A;C snv 3.0E-05 15
rs2201841 0.716 0.440 1 67228519 intron variant A/G;T snv 14
rs879761216 0.732 0.480 1 23875429 frameshift variant TT/C;T delins 14
rs7528684 0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 13