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rs137852567

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137852567(A;G)
Make rs137852567(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67717595
GeneAR
is asnp
is mentioned by
dbSNPrs137852567
ebirs137852567
HLIrs137852567
Exacrs137852567
Varsomers137852567
Maprs137852567
PheGenIrs137852567
hapmaprs137852567
1000 genomesrs137852567
hgdprs137852567
ensemblrs137852567
gopubmedrs137852567
geneviewrs137852567
scholarrs137852567
googlers137852567
pharmgkbrs137852567
gwascentralrs137852567
openSNPrs137852567
23andMers137852567
23andMe allrs137852567
SNP Nexus

SNPshotrs137852567
SNPdbers137852567
MSV3drs137852567
GWAS Ctlgrs137852567
Max Magnitude0
OMIM313700
Desc
Variant0008
Relatedalso
ClinVar
Risk rs137852567(G;G)
Alt rs137852567(G;G)
Reference rs137852567(A;A)
Significance Pathogenic
Disease Reifenstein syndrome
Variation info
Gene AR
CLNDBN Reifenstein syndrome
Reversed 0
HGVS NC_000023.10:g.66937437A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010484.2,