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rs137852585

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137852585(G;G)
Make rs137852585(G;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67711639
GeneAR
is asnp
is mentioned by
dbSNPrs137852585
ebirs137852585
HLIrs137852585
Exacrs137852585
Varsomers137852585
Maprs137852585
PheGenIrs137852585
hapmaprs137852585
1000 genomesrs137852585
hgdprs137852585
ensemblrs137852585
gopubmedrs137852585
geneviewrs137852585
scholarrs137852585
googlers137852585
pharmgkbrs137852585
gwascentralrs137852585
openSNPrs137852585
23andMers137852585
23andMe allrs137852585
SNP Nexus

SNPshotrs137852585
SNPdbers137852585
MSV3drs137852585
GWAS Ctlgrs137852585
Max Magnitude0
OMIM313700
Desc
Variant0034
Relatedalso
ClinVar
Risk rs137852585(G;G)
Alt rs137852585(G;G)
Reference rs137852585(T;T)
Significance Pathogenic
Disease Androgen resistance syndrome
Variation info
Gene AR
CLNDBN Androgen resistance syndrome
Reversed 0
HGVS NC_000023.10:g.66931481T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010511.4,