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rs137852587

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137852587(A;A)
Make rs137852587(A;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67643387
GeneAR
is asnp
is mentioned by
dbSNPrs137852587
ebirs137852587
HLIrs137852587
Exacrs137852587
Varsomers137852587
Maprs137852587
PheGenIrs137852587
hapmaprs137852587
1000 genomesrs137852587
hgdprs137852587
ensemblrs137852587
gopubmedrs137852587
geneviewrs137852587
scholarrs137852587
googlers137852587
pharmgkbrs137852587
gwascentralrs137852587
openSNPrs137852587
23andMers137852587
23andMe allrs137852587
SNP Nexus

SNPshotrs137852587
SNPdbers137852587
MSV3drs137852587
GWAS Ctlgrs137852587
Max Magnitude0
OMIM313700
Desc
Variant0036
Relatedalso
ClinVar
Risk rs137852587(A;A)
Alt rs137852587(A;A)
Reference rs137852587(T;T)
Significance Pathogenic
Disease Androgen resistance syndrome
Variation info
Gene AR
CLNDBN Androgen resistance syndrome
Reversed 0
HGVS NC_000023.10:g.66863229T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010513.3,