Variant (rsID / SNP)

rs121434388

rs121434388 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RBBP8. Location: chromosome 18, position 20,572,799. Clinical significance in the table: Uncertain significance.

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Reference-table entries

RBBP8Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 18:20572799
Cytoband: 18q11.2
HGVS: NM_002894.3(RBBP8):c.1009A>G (p.Lys337Glu)
Allele change: Missense_K337E

Associated conditions / phenotypes

Carcinoma of pancreas

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.