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rs387906846

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906846(C;T)
Make rs387906846(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position26773716
GeneARID1A
is asnp
is mentioned by
dbSNPrs387906846
ebirs387906846
HLIrs387906846
Exacrs387906846
Varsomers387906846
Maprs387906846
PheGenIrs387906846
hapmaprs387906846
1000 genomesrs387906846
hgdprs387906846
ensemblrs387906846
gopubmedrs387906846
geneviewrs387906846
scholarrs387906846
googlers387906846
pharmgkbrs387906846
gwascentralrs387906846
openSNPrs387906846
23andMers387906846
23andMe allrs387906846
SNP Nexus

SNPshotrs387906846
SNPdbers387906846
MSV3drs387906846
GWAS Ctlgrs387906846
Max Magnitude0
ClinVar
Risk rs387906846(T;T)
Alt rs387906846(T;T)
Reference rs387906846(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene ARID1A
CLNDBN Mental retardation, autosomal dominant 14
Reversed 0
HGVS NC_000001.10:g.27100207C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023229.3,