Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10922106
CFH
0.925 0.080 1 196722334 intron variant A/G snv 0.43 2
rs10922144 1.000 0.040 1 196854170 intron variant C/A;T snv 2
rs10922146 1.000 0.040 1 196865506 intron variant C/T snv 0.19 2
rs10922147
CFHR4
1.000 0.040 1 196908559 intron variant C/G snv 0.22 2
rs11807331
KCNT2
1.000 0.040 1 196458681 intron variant T/C snv 0.33 2
rs12041668
CFH
1.000 0.040 1 196693917 intron variant C/T snv 0.19 2
rs12047098 1.000 0.040 1 196865976 intron variant T/C snv 0.19 2
rs12065463
KCNT2
1.000 0.040 1 196495624 intron variant T/C snv 0.33 2
rs12069983
KCNT2
1.000 0.040 1 196418611 intron variant C/A snv 0.27 2
rs12069990
KCNT2
1.000 0.040 1 196418679 intron variant C/T snv 0.27 2
rs12124794
CFH
1.000 0.040 1 196692408 intron variant A/G;T snv 2
rs12729649
KCNT2
1.000 0.040 1 196418502 intron variant G/A snv 0.61 2
rs12755054
CFHR5
1.000 0.040 1 196977900 intron variant T/A;C snv 2
rs1329428
CFH
0.807 0.160 1 196733680 intron variant C/T snv 0.44 2
rs1410996
CFH
0.807 0.240 1 196727803 intron variant G/A snv 0.46 2
rs1538687
KCNT2
1.000 0.040 1 196428645 intron variant C/T snv 0.62 2
rs1576340
CFH
1.000 0.040 1 196729581 intron variant G/T snv 0.19 2
rs1750311
CFHR5
1.000 0.040 1 196985095 intron variant C/A snv 0.43 2
rs1759016
CFHR5
1.000 0.040 1 196983368 intron variant C/T snv 0.43 2
rs1769996
KCNT2
1.000 0.040 1 196383911 intron variant C/T snv 0.64 2
rs1831281
CFH
1.000 0.040 1 196711684 intron variant C/T snv 0.20 2
rs1963605 1.000 0.040 1 196853038 intron variant C/A;T snv 2
rs1964645 1.000 0.040 1 196852884 intron variant T/A;C snv 2
rs2071277
NOTCH4
0.882 0.200 6 32203906 intron variant T/C snv 0.48 0.46 2
rs2284664
CFH
0.925 0.040 1 196733395 intron variant C/A;T snv 2