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rs137852594

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852594(C;T)
Make rs137852594(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67723745
GeneAR
is asnp
is mentioned by
dbSNPrs137852594
ebirs137852594
HLIrs137852594
Exacrs137852594
Varsomers137852594
Maprs137852594
PheGenIrs137852594
hapmaprs137852594
1000 genomesrs137852594
hgdprs137852594
ensemblrs137852594
gopubmedrs137852594
geneviewrs137852594
scholarrs137852594
googlers137852594
pharmgkbrs137852594
gwascentralrs137852594
openSNPrs137852594
23andMers137852594
23andMe allrs137852594
SNP Nexus

SNPshotrs137852594
SNPdbers137852594
MSV3drs137852594
GWAS Ctlgrs137852594
Max Magnitude0
OMIM313700
Desc
Variant0048
Relatedalso
ClinVar
Risk rs137852594(T;T)
Alt rs137852594(T;T)
Reference rs137852594(C;C)
Significance Pathogenic
Disease Androgen resistance syndrome
Variation info
Gene AR
CLNDBN Androgen resistance syndrome
Reversed 0
HGVS NC_000023.10:g.66943587C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010524.3,