Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs61816761
FLG ; FLG-AS1
0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 24
rs121907900
WT1
0.763 0.200 11 32392020 missense variant G/A snv 7
rs137852569
AR
0.752 0.320 X 67686030 missense variant G/A snv 9.4E-06 3
rs1057517779
NR5A1
0.851 0.160 9 124493083 missense variant G/A snv 2
rs121434250
SRD5A2
0.790 0.200 2 31529419 missense variant C/G;T snv 1.4E-04 1.5E-04 2
rs9332964
SRD5A2
0.763 0.240 2 31529325 missense variant C/T snv 4.7E-04 1.6E-04 2
rs121918508
FGFR2
0.851 0.360 10 121488035 missense variant C/T snv 1
rs9332960
SRD5A2
0.882 0.200 2 31580885 stop gained G/A snv 1.7E-05 1
rs9332967
SRD5A2
0.790 0.200 2 31526224 missense variant C/T snv 2.3E-04 1.1E-04 1
rs1037084691
WT1
0.827 0.160 11 32392031 missense variant C/G;T snv 1