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rs137852588

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852588(C;T)
Make rs137852588(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67643284
GeneAR
is asnp
is mentioned by
dbSNPrs137852588
ebirs137852588
HLIrs137852588
Exacrs137852588
Varsomers137852588
Maprs137852588
PheGenIrs137852588
hapmaprs137852588
1000 genomesrs137852588
hgdprs137852588
ensemblrs137852588
gopubmedrs137852588
geneviewrs137852588
scholarrs137852588
googlers137852588
pharmgkbrs137852588
gwascentralrs137852588
openSNPrs137852588
23andMers137852588
23andMe allrs137852588
SNP Nexus

SNPshotrs137852588
SNPdbers137852588
MSV3drs137852588
GWAS Ctlgrs137852588
Max Magnitude0
OMIM313700
Desc
Variant0037
Relatedalso
ClinVar
Risk rs137852588(T;T)
Alt rs137852588(T;T)
Reference rs137852588(C;C)
Significance Pathogenic
Disease Hypospadias 1
Variation info
Gene AR
CLNDBN Hypospadias 1, X-linked
Reversed 0
HGVS NC_000023.10:g.66863126C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010514.4,