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rs6162

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs6162(A;A)
Make rs6162(A;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position102837224
GeneCYP17A1
is asnp
is mentioned by
dbSNPrs6162
dbSNP (classic)rs6162
ClinGenrs6162
ebirs6162
HLIrs6162
Exacrs6162
Gnomadrs6162
Varsomers6162
LitVarrs6162
Maprs6162
PheGenIrs6162
Biobankrs6162
1000 genomesrs6162
hgdprs6162
ensemblrs6162
geneviewrs6162
scholarrs6162
googlers6162
pharmgkbrs6162
gwascentralrs6162
openSNPrs6162
23andMers6162
SNPshotrs6162
SNPdbers6162
MSV3drs6162
GWAS Ctlgrs6162
GMAF0.4288
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 23186779] Molecular markers in Key Steroidogenic Pathways, Circulating steroid levels and Prostate Cancer progression


[PMID 18163429OA-icon.png] Genetic polymorphisms in CYP17, CYP3A4, CYP19A1, SRD5A2, IGF-1, and IGFBP-3 and prostate cancer risk in African-American men: the Flint Men's Health Study.


[PMID 20411041OA-icon.png] Common Variation in the CYP17A1 and IFIT1 Genes on Chromosome 10 Does Not Contribute to the Risk of Endometriosis.


[PMID 21656827] CYP17 gene polymorphisms and prostate cancer risk: a meta-analysis based on 38 independent studies.


[PMID 22714708] Genetic polymorphisms of CYP17A1 in steroidogenesis pathway are associated with risk of progression to castration-resistant prostate cancer in Japanese men receiving androgen deprivation therapy.


ClinVar
Risk rs6162(A;A)
Alt rs6162(A;A)
Reference Rs6162(G;G)
Significance Non-pathogenic
Disease Congenital adrenal hyperplasia
Variation info
Gene CYP17A1
CLNDBN Congenital adrenal hyperplasia
Reversed 0
HGVS NC_000010.10:g.104596981G>A
CLNSRC
CLNACC RCV000403468.1,