Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34920465 0.807 0.160 1 22373858 intergenic variant A/G snv 0.24 7
rs2252865
RERE
0.851 0.040 1 8362616 intron variant T/C snv 0.72 6
rs6684375 1 22379941 regulatory region variant C/T snv 0.20 4
rs12568930 1.000 0.040 1 22375738 intergenic variant T/C snv 0.21 3
rs2235529
WNT4
1.000 0.040 1 22123994 intron variant C/T snv 0.13 3
rs7524102 0.882 0.160 1 22371954 intergenic variant A/G snv 0.21 3
rs12741884 1 22268202 downstream gene variant G/A;C snv 2
rs3765350
WNT4
1 22120823 intron variant A/G snv 0.22 2
rs3920498
LOC105376850
1.000 0.040 1 22166394 intergenic variant G/C snv 0.19 2
rs7521902
LOC105376850
1.000 0.040 1 22164231 intergenic variant C/A snv 0.22 2
rs10493013 1 22376542 regulatory region variant T/C snv 0.20 1
rs10737462
WNT4
1 22118482 3 prime UTR variant C/T snv 0.22 1
rs12044944
FMN2
1 240418353 intron variant C/T snv 0.18 1
rs12407028
GNG12-AS1 ; WLS
1 68182033 intron variant T/A;C snv 0.35 1
rs12408576
CTPS1
1 40998765 intron variant A/G;T snv 1
rs12742784 1.000 0.080 1 22355873 intergenic variant C/A;T snv 1
rs1430740
GNG12-AS1 ; WLS
1 68191827 intron variant T/C snv 0.58 1
rs1430742
WLS ; GNG12-AS1
1 68169392 intron variant T/C snv 0.18 1
rs17131547
TGFBR3
1 91745463 intron variant G/A snv 5.0E-02 1
rs185048405
SLC30A10 ; LOC105372926
1 219865483 intron variant C/T snv 1
rs2566752
WLS ; GNG12-AS1
1.000 0.080 1 68191014 intron variant T/A;C snv 1
rs2566755
WLS ; GNG12-AS1
1 68169707 intron variant T/C snv 0.19 1
rs3971300 1 22158082 downstream gene variant T/C snv 0.33 1
rs4846580
SLC30A10 ; LOC105372926
1 219724599 intron variant G/A snv 0.40 1
rs56318008
LOC105376845 ; WNT4
0.925 0.120 1 22143914 5 prime UTR variant C/T snv 0.13 1