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rs9332975

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs9332975(A;G)
Make rs9332975(G;G)
ReferenceGRCh38 38.1/142
Chromosome2
Position31525347
GeneSRD5A2
is asnp
is mentioned by
dbSNPrs9332975
dbSNP (classic)rs9332975
ClinGenrs9332975
ebirs9332975
HLIrs9332975
Exacrs9332975
Gnomadrs9332975
Varsomers9332975
LitVarrs9332975
Maprs9332975
PheGenIrs9332975
Biobankrs9332975
1000 genomesrs9332975
hgdprs9332975
ensemblrs9332975
geneviewrs9332975
scholarrs9332975
googlers9332975
pharmgkbrs9332975
gwascentralrs9332975
openSNPrs9332975
23andMers9332975
SNPshotrs9332975
SNPdbers9332975
MSV3drs9332975
GWAS Ctlgrs9332975
GMAF0.1276
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 23499746] SRD5A1 and SRD5A2 are associated with treatment for benign prostatic hyperplasia with the combination of 5α-reductase inhibitors and α-adrenergic receptor antagonists


ClinVar
Risk rs9332975(G;G)
Alt rs9332975(G;G)
Reference Rs9332975(A;A)
Significance Probable-non-pathogenic
Disease not provided 3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency
Variation info
Gene SRD5A2
CLNDBN not provided 3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency
Reversed 1
HGVS NC_000002.11:g.31750417T>C
CLNSRC ClinVar
CLNACC RCV000083668.1, RCV000365985.1,