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rs794727977

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794727977(C;T)
Make rs794727977(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position157148764
GeneARID1B
is asnp
is mentioned by
dbSNPrs794727977
ebirs794727977
HLIrs794727977
Exacrs794727977
Varsomers794727977
Maprs794727977
PheGenIrs794727977
hapmaprs794727977
1000 genomesrs794727977
hgdprs794727977
ensemblrs794727977
gopubmedrs794727977
geneviewrs794727977
scholarrs794727977
googlers794727977
pharmgkbrs794727977
gwascentralrs794727977
openSNPrs794727977
23andMers794727977
23andMe allrs794727977
SNP Nexus

SNPshotrs794727977
SNPdbers794727977
MSV3drs794727977
GWAS Ctlgrs794727977
Max Magnitude0
ClinVar
Risk rs794727977(T;T)
Alt rs794727977(T;T)
Reference rs794727977(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene ARID1B
CLNDBN Mental retardation, autosomal dominant 12
Reversed 0
HGVS NC_000006.11:g.157469898C>T
CLNSRC
CLNACC RCV000180674.1,