Have questions? Visit https://www.reddit.com/r/SNPedia

rs137852574

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137852574(G;G)
Make rs137852574(G;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67723688
GeneAR
is asnp
is mentioned by
dbSNPrs137852574
ebirs137852574
HLIrs137852574
Exacrs137852574
Varsomers137852574
Maprs137852574
PheGenIrs137852574
hapmaprs137852574
1000 genomesrs137852574
hgdprs137852574
ensemblrs137852574
gopubmedrs137852574
geneviewrs137852574
scholarrs137852574
googlers137852574
pharmgkbrs137852574
gwascentralrs137852574
openSNPrs137852574
23andMers137852574
23andMe allrs137852574
SNP Nexus

SNPshotrs137852574
SNPdbers137852574
MSV3drs137852574
GWAS Ctlgrs137852574
Max Magnitude0
OMIM313700
Desc
Variant0020
Relatedalso
ClinVar
Risk rs137852574(G;G)
Alt rs137852574(G;G)
Reference rs137852574(T;T)
Significance Pathogenic
Disease Hypospadias 1
Variation info
Gene AR
CLNDBN Hypospadias 1, X-linked
Reversed 0
HGVS NC_000023.10:g.66943530T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010498.3,