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rs398122907

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TTCT;TTCT) 0 common in clinvar
Make rs398122907(-;-)
Make rs398122907(-;TTCT)
ReferenceGRCh38 38.1/141
Chromosome3
Position41233615
GeneCTNNB1
is asnp
is mentioned by
dbSNPrs398122907
ebirs398122907
HLIrs398122907
Exacrs398122907
Varsomers398122907
Maprs398122907
PheGenIrs398122907
hapmaprs398122907
1000 genomesrs398122907
hgdprs398122907
ensemblrs398122907
gopubmedrs398122907
geneviewrs398122907
scholarrs398122907
googlers398122907
pharmgkbrs398122907
gwascentralrs398122907
openSNPrs398122907
23andMers398122907
23andMe allrs398122907
SNP Nexus

SNPshotrs398122907
SNPdbers398122907
MSV3drs398122907
GWAS Ctlgrs398122907
Max Magnitude0
ClinVar
Risk rs398122907(;)
Alt rs398122907(;)
Reference rs398122907(TTCT;TTCT)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene CTNNB1
CLNDBN Mental retardation, autosomal dominant 19
Reversed 0
HGVS NC_000003.11:g.41275106_41275109delTTCT
CLNSRC OMIM Allelic Variant
CLNACC RCV000032858.28,