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rs387906845

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906845(C;T)
Make rs387906845(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position26766246
GeneARID1A
is asnp
is mentioned by
dbSNPrs387906845
ebirs387906845
HLIrs387906845
Exacrs387906845
Varsomers387906845
Maprs387906845
PheGenIrs387906845
hapmaprs387906845
1000 genomesrs387906845
hgdprs387906845
ensemblrs387906845
gopubmedrs387906845
geneviewrs387906845
scholarrs387906845
googlers387906845
pharmgkbrs387906845
gwascentralrs387906845
openSNPrs387906845
23andMers387906845
23andMe allrs387906845
SNP Nexus

SNPshotrs387906845
SNPdbers387906845
MSV3drs387906845
GWAS Ctlgrs387906845
Max Magnitude0
ClinVar
Risk rs387906845(T;T)
Alt rs387906845(T;T)
Reference rs387906845(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene ARID1A
CLNDBN Mental retardation, autosomal dominant 14
Reversed 0
HGVS NC_000001.10:g.27092737C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023228.3,