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rs137852597

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137852597(C;C)
Make rs137852597(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67722973
GeneAR
is asnp
is mentioned by
dbSNPrs137852597
ebirs137852597
HLIrs137852597
Exacrs137852597
Varsomers137852597
Maprs137852597
PheGenIrs137852597
hapmaprs137852597
1000 genomesrs137852597
hgdprs137852597
ensemblrs137852597
gopubmedrs137852597
geneviewrs137852597
scholarrs137852597
googlers137852597
pharmgkbrs137852597
gwascentralrs137852597
openSNPrs137852597
23andMers137852597
23andMe allrs137852597
SNP Nexus

SNPshotrs137852597
SNPdbers137852597
MSV3drs137852597
GWAS Ctlgrs137852597
Max Magnitude0
OMIM313700
Desc
Variant0052
Relatedalso
ClinVar
Risk rs137852597(C;C)
Alt rs137852597(C;C)
Reference rs137852597(T;T)
Significance Pathogenic
Disease Androgen resistance syndrome
Variation info
Gene AR
CLNDBN Androgen resistance syndrome
Reversed 0
HGVS NC_000023.10:g.66942815T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000010528.2,