Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs191281603
CFHR5
0.851 0.040 1 196989521 intron variant C/G;T snv 4.6E-03 4
rs2842339
RAD51B
0.851 0.040 14 68520282 intron variant G/A snv 0.90 4
rs3750846
ARMS2 ; LOC105378525
0.851 0.040 10 122456049 intron variant T/C snv 0.24 4
rs55975637
COL8A1
0.851 0.040 3 99701009 intron variant G/A;T snv 4
rs5754227
SYN3
0.851 0.040 22 32709831 intron variant T/C snv 0.26 4
rs5817082
CETP
0.851 0.040 16 56963437 intron variant -/A delins 4
rs61941274
ACAD10
0.827 0.160 12 111694806 intron variant G/A;T snv 4
rs61985136
RAD51B
0.851 0.040 14 68302482 intron variant C/T snv 0.52 4
rs62247658
ADAMTS9-AS2
0.851 0.040 3 64729479 intron variant C/T snv 0.42 4
rs6565597
NPLOC4
0.851 0.040 17 81559795 intron variant C/T snv 0.30 4
rs67538026
CNN2
0.851 0.040 19 1031439 intron variant C/T snv 0.37 4
rs7088058
PLEKHA1
0.851 0.040 10 122389836 intron variant C/T snv 0.32 4
rs71507014
TRPM3
0.851 0.040 9 70823689 intron variant -/C;CC delins 4
rs7803454
PILRA
0.851 0.040 7 100393925 intron variant C/T snv 0.14 4
rs8135665
LOC105373027 ; SLC16A8
0.851 0.040 22 38080269 intron variant C/T snv 0.24 4
rs1329428
CFH
0.807 0.160 1 196733680 intron variant C/T snv 0.44 3
rs2284665
HTRA1
0.882 0.040 10 122467114 intron variant G/A;T snv 3
rs2292626
PLEKHA1
0.925 0.120 10 122427198 intron variant C/T snv 0.46 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
rs12153855
TNXB
0.776 0.320 6 32107027 intron variant T/C snv 0.11 2
rs1831282
CFH
1.000 0.040 1 196704863 intron variant A/C snv 0.62 2
rs2421016
PLEKHA1
0.925 0.120 10 122407996 intron variant C/T snv 0.46 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