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rs137852564

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852564(A;A)
Make rs137852564(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67722976
GeneAR
is asnp
is mentioned by
dbSNPrs137852564
ebirs137852564
HLIrs137852564
Exacrs137852564
Varsomers137852564
Maprs137852564
PheGenIrs137852564
hapmaprs137852564
1000 genomesrs137852564
hgdprs137852564
ensemblrs137852564
gopubmedrs137852564
geneviewrs137852564
scholarrs137852564
googlers137852564
pharmgkbrs137852564
gwascentralrs137852564
openSNPrs137852564
23andMers137852564
23andMe allrs137852564
SNP Nexus

SNPshotrs137852564
SNPdbers137852564
MSV3drs137852564
GWAS Ctlgrs137852564
Max Magnitude0
OMIM313700
Desc
Variant0005
Relatedalso
OMIM313700
Desc
Variant0018
Relatedalso
ClinVar
Risk rs137852564(A,T;A,T)
Alt rs137852564(A,T;A,T)
Reference rs137852564(G;G)
Significance Pathogenic
Disease Androgen resistance syndrome Reifenstein syndrome
Variation info
Gene AR
CLNDBN Androgen resistance syndrome Reifenstein syndrome
Reversed 0
HGVS NC_000023.10:g.66942818G>A; NC_000023.10:g.66942818G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010480.6, RCV000010496.2,