Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs2284664
CFH
0.925 0.040 1 196733395 intron variant C/A;T snv 2
rs2878557
KCNT2
1.000 0.040 1 196433643 intron variant T/C snv 0.61 2
rs3753395
CFH
0.882 0.120 1 196717522 intron variant A/G;T snv 2
rs3855964
KCNT2
1.000 0.040 1 196414986 intron variant T/G snv 0.70 2
rs3927686
KCNT2
1.000 0.040 1 196416519 intron variant T/C snv 0.70 2
rs3928857
KCNT2
1.000 0.040 1 196414471 intron variant T/C snv 0.64 2
rs4657825 1.000 0.040 1 196615191 intergenic variant A/G;T snv 2
rs4915318
LOC105371675
1.000 0.040 1 196927958 intergenic variant C/A;T snv 2
rs4915559
CFHR4 ; LOC105371675
1.000 0.040 1 196917640 intron variant T/A;C snv 2
rs529825
CFH
1.000 0.040 1 196665976 intron variant G/A snv 0.40 2