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rs137852571

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852571(A;A)
Make rs137852571(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67717495
GeneAR
is asnp
is mentioned by
dbSNPrs137852571
ebirs137852571
HLIrs137852571
Exacrs137852571
Varsomers137852571
Maprs137852571
PheGenIrs137852571
hapmaprs137852571
1000 genomesrs137852571
hgdprs137852571
ensemblrs137852571
gopubmedrs137852571
geneviewrs137852571
scholarrs137852571
googlers137852571
pharmgkbrs137852571
gwascentralrs137852571
openSNPrs137852571
23andMers137852571
23andMe allrs137852571
SNP Nexus

SNPshotrs137852571
SNPdbers137852571
MSV3drs137852571
GWAS Ctlgrs137852571
Max Magnitude0
OMIM313700
Desc
Variant0013
Relatedalso
ClinVar
Risk rs137852571(A;A)
Alt rs137852571(A;A)
Reference rs137852571(G;G)
Significance Pathogenic
Disease Malignant tumor of prostate
Variation info
Gene AR
CLNDBN Malignant tumor of prostate
Reversed 0
HGVS NC_000023.10:g.66937337G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010491.4,