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rs137852592

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137852592(C;C)
Make rs137852592(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67721937
GeneAR
is asnp
is mentioned by
dbSNPrs137852592
ebirs137852592
HLIrs137852592
Exacrs137852592
Varsomers137852592
Maprs137852592
PheGenIrs137852592
hapmaprs137852592
1000 genomesrs137852592
hgdprs137852592
ensemblrs137852592
gopubmedrs137852592
geneviewrs137852592
scholarrs137852592
googlers137852592
pharmgkbrs137852592
gwascentralrs137852592
openSNPrs137852592
23andMers137852592
23andMe allrs137852592
SNP Nexus

SNPshotrs137852592
SNPdbers137852592
MSV3drs137852592
GWAS Ctlgrs137852592
Max Magnitude0
OMIM313700
Desc
Variant0044
Relatedalso
ClinVar
Risk rs137852592(C;C)
Alt rs137852592(C;C)
Reference rs137852592(T;T)
Significance Pathogenic
Disease Reifenstein syndrome
Variation info
Gene AR
CLNDBN Reifenstein syndrome
Reversed 0
HGVS NC_000023.10:g.66941779T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000010521.4,