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rs137852575

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852575(C;T)
Make rs137852575(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67545324
GeneAR
is asnp
is mentioned by
dbSNPrs137852575
ebirs137852575
HLIrs137852575
Exacrs137852575
Varsomers137852575
Maprs137852575
PheGenIrs137852575
hapmaprs137852575
1000 genomesrs137852575
hgdprs137852575
ensemblrs137852575
gopubmedrs137852575
geneviewrs137852575
scholarrs137852575
googlers137852575
pharmgkbrs137852575
gwascentralrs137852575
openSNPrs137852575
23andMers137852575
23andMe allrs137852575
SNP Nexus

SNPshotrs137852575
SNPdbers137852575
MSV3drs137852575
GWAS Ctlgrs137852575
Max Magnitude0
OMIM313700
Desc
Variant0021
Relatedalso
ClinVar
Risk rs137852575(T;T)
Alt rs137852575(T;T)
Reference rs137852575(C;C)
Significance Pathogenic
Disease Androgen resistance syndrome
Variation info
Gene AR
CLNDBN Androgen resistance syndrome
Reversed 0
HGVS NC_000023.10:g.66765166C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010499.2,