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rs28933691

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs28933691(A;A)
Make rs28933691(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position47915182
GeneZNF81
is asnp
is mentioned by
dbSNPrs28933691
ebirs28933691
HLIrs28933691
Exacrs28933691
Varsomers28933691
Maprs28933691
PheGenIrs28933691
hapmaprs28933691
1000 genomesrs28933691
hgdprs28933691
ensemblrs28933691
gopubmedrs28933691
geneviewrs28933691
scholarrs28933691
googlers28933691
pharmgkbrs28933691
gwascentralrs28933691
openSNPrs28933691
23andMers28933691
23andMe allrs28933691
SNP Nexus

SNPshotrs28933691
SNPdbers28933691
MSV3drs28933691
GWAS Ctlgrs28933691
Max Magnitude0
OMIM314998
DescMENTAL RETARDATION, X-LINKED 45
Variant0001
Relatedalso


ClinVar
Risk rs28933691(A;A)
Alt rs28933691(A;A)
Reference rs28933691(G;G)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene ZNF81
CLNDBN Mental retardation, X-linked 45
Reversed 0
HGVS NC_000023.10:g.47774581G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010413.3,