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rs137852589

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852589(G;T)
Make rs137852589(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67721857
GeneAR
is asnp
is mentioned by
dbSNPrs137852589
ebirs137852589
HLIrs137852589
Exacrs137852589
Varsomers137852589
Maprs137852589
PheGenIrs137852589
hapmaprs137852589
1000 genomesrs137852589
hgdprs137852589
ensemblrs137852589
gopubmedrs137852589
geneviewrs137852589
scholarrs137852589
googlers137852589
pharmgkbrs137852589
gwascentralrs137852589
openSNPrs137852589
23andMers137852589
23andMe allrs137852589
SNP Nexus

SNPshotrs137852589
SNPdbers137852589
MSV3drs137852589
GWAS Ctlgrs137852589
Max Magnitude0
OMIM313700
Desc
Variant0039
Relatedalso
ClinVar
Risk rs137852589(T;T)
Alt rs137852589(T;T)
Reference rs137852589(G;G)
Significance Pathogenic
Disease Androgen resistance syndrome
Variation info
Gene AR
CLNDBN Androgen resistance syndrome
Reversed 0
HGVS NC_000023.10:g.66941699G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010516.2,