Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2421016
PLEKHA1
0.925 0.120 10 122407996 intron variant C/T snv 0.46 2
rs2588809
RAD51B
0.807 0.160 14 68193711 intron variant T/C snv 0.80 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
rs4915559
CFHR4 ; LOC105371675
1.000 0.040 1 196917640 intron variant T/A;C snv 2
rs493258
ALDH1A2
0.925 0.040 15 58395681 intron variant T/C snv 0.50 2
rs529825
CFH
1.000 0.040 1 196665976 intron variant G/A snv 0.40 2
rs544167
CYP21A2 ; C2
0.925 0.160 6 31922381 intron variant T/G snv 7.3E-02 2
rs550513
NELFE ; CYP21A2
0.925 0.160 6 31952910 intron variant C/T snv 0.12 2
rs550605
C2 ; CYP21A2 ; C2-AS1
0.925 0.160 6 31939370 intron variant T/C snv 9.7E-02 0.12 2
rs6657442 1.000 0.040 1 196868930 intron variant T/C snv 0.19 2
rs6677604
CFH
0.827 0.200 1 196717788 intron variant G/A snv 0.23 2
rs7366238
CFHR4
1.000 0.040 1 196891667 intron variant A/G snv 0.22 2
rs7413265 1.000 0.040 1 196870033 intron variant G/T snv 0.19 2
rs7535696
KCNT2
1.000 0.040 1 196402302 intron variant T/C snv 0.27 2
rs7540032
CFH
0.925 0.080 1 196732154 intron variant C/T snv 0.44 2
rs920915
ALDH1A2
1.000 0.040 15 58396268 intron variant C/G snv 0.55 2
rs10033900
CFI
0.807 0.040 4 109737911 intron variant T/C snv 0.54 1
rs1021636 1.000 0.040 1 196876143 intron variant A/G snv 0.21 1
rs10733086
CFH
1.000 0.040 1 196707805 intron variant A/C;T snv 1
rs10749466
PLEKHA1
1.000 0.040 10 122379288 intron variant A/G snv 0.32 1
rs10754196
KCNT2
1.000 0.040 1 196601576 intron variant A/G snv 0.30 1