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rs137852598

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852598(C;G)
Make rs137852598(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67722948
GeneAR
is asnp
is mentioned by
dbSNPrs137852598
ebirs137852598
HLIrs137852598
Exacrs137852598
Varsomers137852598
Maprs137852598
PheGenIrs137852598
hapmaprs137852598
1000 genomesrs137852598
hgdprs137852598
ensemblrs137852598
gopubmedrs137852598
geneviewrs137852598
scholarrs137852598
googlers137852598
pharmgkbrs137852598
gwascentralrs137852598
openSNPrs137852598
23andMers137852598
23andMe allrs137852598
SNP Nexus

SNPshotrs137852598
SNPdbers137852598
MSV3drs137852598
GWAS Ctlgrs137852598
Max Magnitude0
OMIM313700
Desc
Variant0053
Relatedalso
ClinVar
Risk rs137852598(G,T;G,T)
Alt rs137852598(G,T;G,T)
Reference rs137852598(C;C)
Significance Pathogenic
Disease Androgen resistance syndrome
Variation info
Gene AR
CLNDBN Androgen resistance syndrome
Reversed 0
HGVS NC_000023.10:g.66942790C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010490.4,