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rs797045283

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797045283(C;T)
Make rs797045283(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position157207109
GeneARID1B
is asnp
is mentioned by
dbSNPrs797045283
ebirs797045283
HLIrs797045283
Exacrs797045283
Varsomers797045283
Maprs797045283
PheGenIrs797045283
hapmaprs797045283
1000 genomesrs797045283
hgdprs797045283
ensemblrs797045283
gopubmedrs797045283
geneviewrs797045283
scholarrs797045283
googlers797045283
pharmgkbrs797045283
gwascentralrs797045283
openSNPrs797045283
23andMers797045283
23andMe allrs797045283
SNP Nexus

SNPshotrs797045283
SNPdbers797045283
MSV3drs797045283
GWAS Ctlgrs797045283
Max Magnitude0
ClinVar
Risk rs797045283(T;T)
Alt rs797045283(T;T)
Reference rs797045283(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene ARID1B
CLNDBN Mental retardation, autosomal dominant 12
Reversed 0
HGVS NC_000006.11:g.157528243C>T
CLNSRC
CLNACC RCV000194737.1,