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
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs751377893
F5
0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 65
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs5361 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs11575937 0.653 0.480 1 156136985 missense variant G/A;T snv 29
rs11591147 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs599839 0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs646776 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs35829419 0.689 0.560 1 247425556 missense variant C/A snv 3.9E-02 3.3E-02 23
rs7517847 0.689 0.600 1 67215986 intron variant T/G snv 0.37 19
rs3850641 0.716 0.400 1 173206693 intron variant A/G snv 0.14 17
rs6136 0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 17
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs2890565 0.732 0.440 1 7849677 missense variant C/T snv 8.7E-02 5.6E-02 15