Source: ALL
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
rs10490924
ARMS2 ; LOC105378525
0.716 0.240 10 122454932 missense variant G/T snv 0.26 0.23 16
rs121913059
CFH
0.716 0.280 1 196747245 missense variant C/T snv 1.4E-04 1.9E-04 16
rs121434491
EFEMP1 ; LOC112268416
0.752 0.200 2 55871091 missense variant G/A snv 15
rs11200638
LOC105378525 ; HTRA1
0.724 0.280 10 122461028 non coding transcript exon variant G/A snv 0.23 14
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 13
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 12
rs1555038029
KMT2A
0.776 0.400 11 118477973 stop gained C/A snv 12
rs641153
CFB ; CYP21A2
0.790 0.160 6 31946403 missense variant G/A;T snv 9.6E-02; 4.1E-06 7
rs570618
CFH
0.827 0.040 1 196687934 intron variant T/G snv 0.69 6
rs148060787
BEST1 ; FTH1
0.851 0.080 11 61962853 missense variant C/G;T snv 4.4E-04 5
rs1800995
BEST1 ; LOC107984334
0.851 0.080 11 61955906 missense variant GC/AA mnv 5
rs1805142
BEST1 ; LOC107984334
0.851 0.080 11 61955825 stop gained G/C;T snv 2.7E-05 5
rs1049331
LOC105378525 ; HTRA1
0.851 0.040 10 122461754 synonymous variant C/T snv 0.32 0.23 5
rs281865275
LOC107984334 ; BEST1
0.851 0.080 11 61957397 missense variant C/G;T snv 8.0E-06; 2.8E-05 5
rs2672598
HTRA1 ; LOC105378525
0.851 0.160 10 122461166 non coding transcript exon variant T/C snv 0.49 4
rs2293870
LOC105378525 ; HTRA1
0.851 0.160 10 122461760 synonymous variant G/C;T snv 5.9E-02; 0.32 4
rs10664316
ARMS2 ; LOC105378525
1.000 10 122456869 intron variant -/A;AC ins 7.7E-05 1