Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10903323 0.807 0.160 8 10292057 intron variant A/G snv 0.15 8
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs17465637 0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 11
rs17757541 0.827 0.240 18 63212453 intron variant C/G;T snv 7
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs3819025 0.752 0.480 6 52186476 intron variant G/A snv 0.13 8.5E-02 11
rs755622 0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs3869109 0.851 0.160 6 31216419 intergenic variant A/G;T snv 5
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs112735431 0.683 0.320 17 80385145 missense variant G/A;C snv 2.6E-04; 8.0E-06 24
rs11556924 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs2043211 0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29