Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2066853
AHR
0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 34
rs523349
SRD5A2
0.689 0.440 2 31580636 missense variant G/A;C;T snv 0.66; 4.9E-06 21
rs9332964
SRD5A2
0.763 0.240 2 31529325 missense variant C/T snv 4.7E-04 1.6E-04 10
rs2292596
AHRR
0.827 0.240 5 422840 missense variant C/G;T snv 0.38; 4.0E-06 7
rs2066479
HSD17B3
0.790 0.160 9 96235528 missense variant C/A;G;T snv 7.2E-02 7
rs1110061
NR5A1
0.807 0.200 9 124500523 missense variant C/A;G snv 4.3E-06; 0.10 7
rs121434250
SRD5A2
0.790 0.200 2 31529419 missense variant C/G;T snv 1.4E-04 1.5E-04 7
rs554416372
WT1
0.827 0.160 11 32396397 missense variant C/A;G;T snv 2.0E-05; 8.0E-06; 9.6E-05 5
rs121912530
GTF2A1L ; STON1-GTF2A1L ; LHCGR
0.851 0.160 2 48687923 missense variant A/T snv 7.0E-06 4
rs371701248
NR5A1
0.882 0.160 9 124491156 missense variant C/T snv 1.3E-04 5.6E-05 3
rs1311014616
SRD5A2
0.925 0.040 2 31580733 missense variant C/G snv 8.4E-06 2