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rs797045272

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797045272(C;T)
Make rs797045272(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position157084872
GeneARID1B
is asnp
is mentioned by
dbSNPrs797045272
ebirs797045272
HLIrs797045272
Exacrs797045272
Varsomers797045272
Maprs797045272
PheGenIrs797045272
hapmaprs797045272
1000 genomesrs797045272
hgdprs797045272
ensemblrs797045272
gopubmedrs797045272
geneviewrs797045272
scholarrs797045272
googlers797045272
pharmgkbrs797045272
gwascentralrs797045272
openSNPrs797045272
23andMers797045272
23andMe allrs797045272
SNP Nexus

SNPshotrs797045272
SNPdbers797045272
MSV3drs797045272
GWAS Ctlgrs797045272
Max Magnitude0
ClinVar
Risk rs797045272(T;T)
Alt rs797045272(T;T)
Reference rs797045272(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene ARID1B
CLNDBN Mental retardation, autosomal dominant 12
Reversed 0
HGVS NC_000006.11:g.157406006C>T
CLNSRC
CLNACC RCV000193875.1,