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rs137852590

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137852590(G;G)
Make rs137852590(G;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67545667
GeneAR
is asnp
is mentioned by
dbSNPrs137852590
ebirs137852590
HLIrs137852590
Exacrs137852590
Varsomers137852590
Maprs137852590
PheGenIrs137852590
hapmaprs137852590
1000 genomesrs137852590
hgdprs137852590
ensemblrs137852590
gopubmedrs137852590
geneviewrs137852590
scholarrs137852590
googlers137852590
pharmgkbrs137852590
gwascentralrs137852590
openSNPrs137852590
23andMers137852590
23andMe allrs137852590
SNP Nexus

SNPshotrs137852590
SNPdbers137852590
MSV3drs137852590
GWAS Ctlgrs137852590
Max Magnitude0
OMIM313700
Desc
Variant0042
Relatedalso
ClinVar
Risk rs137852590(G;G)
Alt rs137852590(G;G)
Reference rs137852590(T;T)
Significance Pathogenic
Disease Reifenstein syndrome
Variation info
Gene AR
CLNDBN Reifenstein syndrome
Reversed 0
HGVS NC_000023.10:g.66765509T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010519.4,