Variant (rsID / SNP)

rs376814421

rs376814421 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CREBBP. Location: chromosome 16, position 3,789,571. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

CREBBPConflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 16:3789571
Cytoband: 16p13.3
HGVS: NM_004380.3(CREBBP):c.4280+8T>C
Allele change: Silent

Associated conditions / phenotypes

Rubinstein-Taybi syndrome

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.