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rs137852601

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852601(C;G)
Make rs137852601(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67717526
GeneAR
is asnp
is mentioned by
dbSNPrs137852601
ebirs137852601
HLIrs137852601
Exacrs137852601
Varsomers137852601
Maprs137852601
PheGenIrs137852601
hapmaprs137852601
1000 genomesrs137852601
hgdprs137852601
ensemblrs137852601
gopubmedrs137852601
geneviewrs137852601
scholarrs137852601
googlers137852601
pharmgkbrs137852601
gwascentralrs137852601
openSNPrs137852601
23andMers137852601
23andMe allrs137852601
SNP Nexus

SNPshotrs137852601
SNPdbers137852601
MSV3drs137852601
GWAS Ctlgrs137852601
Max Magnitude0
OMIM313700
Desc
Variant0059
Relatedalso
ClinVar
Risk rs137852601(G;G)
Alt rs137852601(G;G)
Reference rs137852601(C;C)
Significance Pathogenic
Disease Reifenstein syndrome
Variation info
Gene AR
CLNDBN Reifenstein syndrome
Reversed 0
HGVS NC_000023.10:g.66937368C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010535.4,