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rs137852572

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852572(A;A)
Make rs137852572(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67721838
GeneAR
is asnp
is mentioned by
dbSNPrs137852572
ebirs137852572
HLIrs137852572
Exacrs137852572
Varsomers137852572
Maprs137852572
PheGenIrs137852572
hapmaprs137852572
1000 genomesrs137852572
hgdprs137852572
ensemblrs137852572
gopubmedrs137852572
geneviewrs137852572
scholarrs137852572
googlers137852572
pharmgkbrs137852572
gwascentralrs137852572
openSNPrs137852572
23andMers137852572
23andMe allrs137852572
SNP Nexus

SNPshotrs137852572
SNPdbers137852572
MSV3drs137852572
GWAS Ctlgrs137852572
Max Magnitude0
OMIM313700
Desc
Variant0015
Relatedalso
ClinVar
Risk rs137852572(A;A)
Alt rs137852572(A;A)
Reference rs137852572(G;G)
Significance Pathogenic
Disease Androgen resistance syndrome
Variation info
Gene AR
CLNDBN Androgen resistance syndrome
Reversed 0
HGVS NC_000023.10:g.66941680G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010493.2,