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rs137852593

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852593(G;T)
Make rs137852593(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67717484
GeneAR
is asnp
is mentioned by
dbSNPrs137852593
ebirs137852593
HLIrs137852593
Exacrs137852593
Varsomers137852593
Maprs137852593
PheGenIrs137852593
hapmaprs137852593
1000 genomesrs137852593
hgdprs137852593
ensemblrs137852593
gopubmedrs137852593
geneviewrs137852593
scholarrs137852593
googlers137852593
pharmgkbrs137852593
gwascentralrs137852593
openSNPrs137852593
23andMers137852593
23andMe allrs137852593
SNP Nexus

SNPshotrs137852593
SNPdbers137852593
MSV3drs137852593
GWAS Ctlgrs137852593
GMAF0.0
Max Magnitude0
OMIM313700
Desc
Variant0047
Relatedalso
ClinVar
Risk rs137852593(A,C,T;A,C,T)
Alt rs137852593(A,C,T;A,C,T)
Reference rs137852593(G;G)
Significance Pathogenic
Disease Prostate cancer susceptibility
Variation info
Gene AR
CLNDBN Prostate cancer susceptibility
Reversed 0
HGVS NC_000023.10:g.66937326G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010523.3,