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rs137852596

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852596(A;A)
Make rs137852596(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67643371
GeneAR
is asnp
is mentioned by
dbSNPrs137852596
ebirs137852596
HLIrs137852596
Exacrs137852596
Varsomers137852596
Maprs137852596
PheGenIrs137852596
hapmaprs137852596
1000 genomesrs137852596
hgdprs137852596
ensemblrs137852596
gopubmedrs137852596
geneviewrs137852596
scholarrs137852596
googlers137852596
pharmgkbrs137852596
gwascentralrs137852596
openSNPrs137852596
23andMers137852596
23andMe allrs137852596
SNP Nexus

SNPshotrs137852596
SNPdbers137852596
MSV3drs137852596
GWAS Ctlgrs137852596
Max Magnitude0
OMIM313700
Desc
Variant0051
Relatedalso
ClinVar
Risk rs137852596(A;A)
Alt rs137852596(A;A)
Reference rs137852596(G;G)
Significance Pathogenic
Disease Androgen resistance syndrome
Variation info
Gene AR
CLNDBN Androgen resistance syndrome
Reversed 0
HGVS NC_000023.10:g.66863213G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010527.2,