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rs137852586

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852586(G;T)
Make rs137852586(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67643378
GeneAR
is asnp
is mentioned by
dbSNPrs137852586
ebirs137852586
HLIrs137852586
Exacrs137852586
Varsomers137852586
Maprs137852586
PheGenIrs137852586
hapmaprs137852586
1000 genomesrs137852586
hgdprs137852586
ensemblrs137852586
gopubmedrs137852586
geneviewrs137852586
scholarrs137852586
googlers137852586
pharmgkbrs137852586
gwascentralrs137852586
openSNPrs137852586
23andMers137852586
23andMe allrs137852586
SNP Nexus

SNPshotrs137852586
SNPdbers137852586
MSV3drs137852586
GWAS Ctlgrs137852586
Max Magnitude0
OMIM313700
Desc
Variant0035
Relatedalso
ClinVar
Risk rs137852586(T;T)
Alt rs137852586(T;T)
Reference rs137852586(G;G)
Significance Pathogenic
Disease Androgen resistance syndrome
Variation info
Gene AR
CLNDBN Androgen resistance syndrome
Reversed 0
HGVS NC_000023.10:g.66863220G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010512.2,