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rs797045278

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797045278(C;T)
Make rs797045278(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position157200930
GeneARID1B
is asnp
is mentioned by
dbSNPrs797045278
ebirs797045278
HLIrs797045278
Exacrs797045278
Varsomers797045278
Maprs797045278
PheGenIrs797045278
hapmaprs797045278
1000 genomesrs797045278
hgdprs797045278
ensemblrs797045278
gopubmedrs797045278
geneviewrs797045278
scholarrs797045278
googlers797045278
pharmgkbrs797045278
gwascentralrs797045278
openSNPrs797045278
23andMers797045278
23andMe allrs797045278
SNP Nexus

SNPshotrs797045278
SNPdbers797045278
MSV3drs797045278
GWAS Ctlgrs797045278
Max Magnitude0
ClinVar
Risk rs797045278(T;T)
Alt rs797045278(T;T)
Reference rs797045278(C;C)
Significance Probable-Pathogenic
Disease Mental retardation
Variation info
Gene ARID1B
CLNDBN Mental retardation, autosomal dominant 12
Reversed 0
HGVS NC_000006.11:g.157522064C>T
CLNSRC
CLNACC RCV000193003.1,