Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10737680
CFH
0.827 0.080 1 196710325 intron variant A/C snv 0.44 7
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 7
rs10922109
CFH
0.827 0.080 1 196735502 intron variant C/A snv 0.46 6
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 5
rs1410996
CFH
0.807 0.240 1 196727803 intron variant G/A snv 0.46 5
rs570618
CFH
0.827 0.040 1 196687934 intron variant T/G snv 0.69 5
rs800292
CFH
0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 5
rs121913059
CFH
0.716 0.280 1 196747245 missense variant C/T snv 1.4E-04 1.9E-04 4
rs148553336 0.851 0.040 1 196644043 intergenic variant T/C snv 7.7E-03 4
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 4
rs187328863
KCNT2
0.851 0.040 1 196411028 intron variant C/T snv 1.6E-02 4
rs191281603
CFHR5
0.851 0.040 1 196989521 intron variant C/G;T snv 4.6E-03 4
rs2274700
CFH
0.776 0.240 1 196713817 synonymous variant G/A;C;T snv 0.44 4
rs35292876
CFH
0.851 0.040 1 196737512 synonymous variant C/T snv 1.0E-02 8.6E-03 4
rs61818925 0.851 0.040 1 196846320 upstream gene variant T/G snv 0.67 4
rs1329428
CFH
0.807 0.160 1 196733680 intron variant C/T snv 0.44 3
rs6677604
CFH
0.827 0.200 1 196717788 intron variant G/A snv 0.23 3
rs10922106
CFH
0.925 0.080 1 196722334 intron variant A/G snv 0.43 2
rs1831282
CFH
1.000 0.040 1 196704863 intron variant A/C snv 0.62 2
rs3753395
CFH
0.882 0.120 1 196717522 intron variant A/G;T snv 2
rs4915559
CFHR4 ; LOC105371675
1.000 0.040 1 196917640 intron variant T/A;C snv 2
rs7535263
CFH
0.925 0.080 1 196713216 intron variant G/A;C snv 2
rs7540032
CFH
0.925 0.080 1 196732154 intron variant C/T snv 0.44 2
rs10494745
CFHR4 ; LOC105371675
1.000 0.040 1 196918327 missense variant G/A snv 8.0E-02 7.4E-02 1
rs1061147
CFH
1.000 0.040 1 196685194 synonymous variant A/C snv 0.68 0.62 1