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rs137852563

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852563(A;A)
Make rs137852563(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67711673
GeneAR
is asnp
is mentioned by
dbSNPrs137852563
ebirs137852563
HLIrs137852563
Exacrs137852563
Varsomers137852563
Maprs137852563
PheGenIrs137852563
hapmaprs137852563
1000 genomesrs137852563
hgdprs137852563
ensemblrs137852563
gopubmedrs137852563
geneviewrs137852563
scholarrs137852563
googlers137852563
pharmgkbrs137852563
gwascentralrs137852563
openSNPrs137852563
23andMers137852563
23andMe allrs137852563
SNP Nexus

SNPshotrs137852563
SNPdbers137852563
MSV3drs137852563
GWAS Ctlgrs137852563
Max Magnitude0
OMIM313700
Desc
Variant0004
Relatedalso
ClinVar
Risk rs137852563(A;A)
Alt rs137852563(A;A)
Reference rs137852563(G;G)
Significance Pathogenic
Disease Androgen resistance syndrome
Variation info
Gene AR
CLNDBN Androgen resistance syndrome
Reversed 0
HGVS NC_000023.10:g.66931515G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010479.2,