Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
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
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs35829419 0.689 0.560 1 247425556 missense variant C/A snv 3.9E-02 3.3E-02 23
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs6136 0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 17
rs800292
CFH
0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 33
rs8192284 0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs17235409 0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs1801278 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38
rs1990760 0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 33
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs2305948
KDR
0.732 0.400 4 55113391 missense variant C/A;T snv 4.0E-06; 0.11 18
rs3733197 0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 13