Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4730775
WNT2
0.851 0.200 7 117277064 3 prime UTR variant C/T snv 0.41 1
rs394563
ZC3H12D
1.000 0.120 6 149475878 intron variant T/C;G snv 1
rs38904 1.000 0.120 7 117252792 intergenic variant T/C snv 0.52 2
rs9525927 0.925 0.160 13 44268367 regulatory region variant G/A snv 0.80 2
rs2598107
SFRP4 ; EPDR1
1.000 0.120 7 37933412 intron variant C/T snv 0.34 2
rs6016142 1.000 0.120 20 39672165 intergenic variant C/T snv 7.8E-02 3
rs7524102 0.882 0.160 1 22371954 intergenic variant A/G snv 0.21 3
rs7838717
BOP1
1.000 0.120 8 144280310 intron variant C/T snv 0.30 3