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rs137852573

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852573(A;A)
Make rs137852573(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67686064
GeneAR
is asnp
is mentioned by
dbSNPrs137852573
ebirs137852573
HLIrs137852573
Exacrs137852573
Varsomers137852573
Maprs137852573
PheGenIrs137852573
hapmaprs137852573
1000 genomesrs137852573
hgdprs137852573
ensemblrs137852573
gopubmedrs137852573
geneviewrs137852573
scholarrs137852573
googlers137852573
pharmgkbrs137852573
gwascentralrs137852573
openSNPrs137852573
23andMers137852573
23andMe allrs137852573
SNP Nexus

SNPshotrs137852573
SNPdbers137852573
MSV3drs137852573
GWAS Ctlgrs137852573
Max Magnitude0
OMIM313700
Desc
Variant0016
Relatedalso
ClinVar
Risk rs137852573(A;A)
Alt rs137852573(A;A)
Reference Rs137852573(G;G)
Significance Pathogenic
Disease Reifenstein syndrome
Variation info
Gene AR
CLNDBN Reifenstein syndrome
Reversed 0
HGVS NC_000023.10:g.66905906G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010494.3,