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rs137852569

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852569(A;A)
Make rs137852569(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67686030
GeneAR
is asnp
is mentioned by
dbSNPrs137852569
ebirs137852569
HLIrs137852569
Exacrs137852569
Varsomers137852569
Maprs137852569
PheGenIrs137852569
hapmaprs137852569
1000 genomesrs137852569
hgdprs137852569
ensemblrs137852569
gopubmedrs137852569
geneviewrs137852569
scholarrs137852569
googlers137852569
pharmgkbrs137852569
gwascentralrs137852569
openSNPrs137852569
23andMers137852569
23andMe allrs137852569
SNP Nexus

SNPshotrs137852569
SNPdbers137852569
MSV3drs137852569
GWAS Ctlgrs137852569
Max Magnitude0
OMIM313700
Desc
Variant0011
Relatedalso
ClinVar
Risk rs137852569(A;A)
Alt rs137852569(A;A)
Reference rs137852569(G;G)
Significance Pathogenic
Disease Reifenstein syndrome
Variation info
Gene AR
CLNDBN Reifenstein syndrome
Reversed 0
HGVS NC_000023.10:g.66905872G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010487.2,