Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10159239 0.882 0.040 1 247443750 intron variant G/A snv 0.57 3
rs1044925 0.827 0.120 1 179354603 3 prime UTR variant C/A;G snv 6
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs10754558 0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 20
rs10911021 0.807 0.160 1 182112825 intron variant C/T snv 0.36 11
rs10918859 0.882 0.040 1 162199478 intron variant G/A snv 0.16 3
rs10920501 0.827 0.120 1 190092815 downstream gene variant A/T snv 0.18 5
rs1131498 0.732 0.360 1 169707345 missense variant A/G snv 0.21 0.22 13
rs11591147 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs12040273 0.882 0.040 1 230063651 intron variant C/T snv 0.28 3
rs12041331 0.776 0.200 1 156899922 intron variant G/A snv 0.19 11
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12567209 0.807 0.080 1 162066689 upstream gene variant G/A snv 8.6E-02 6
rs12740374 0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 16
rs138760780 0.882 0.040 1 205515245 intron variant C/T snv 1.5E-02 3
rs142648132
MTR
0.827 0.160 1 236816521 missense variant G/A;C;T snv 8.4E-04; 2.4E-05 5
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs16847548 0.807 0.120 1 162065484 upstream gene variant T/C snv 0.22 8
rs17465637 0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 11
rs1748195 0.851 0.120 1 62583922 intron variant C/G;T snv 8
rs17568 0.752 0.320 1 1212042 synonymous variant C/T snv 0.37 0.31 12
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
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