Variant (rsID / SNP)

rs9344

rs9344 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCND1. Location: chromosome 11, position 69,462,910. Clinical significance in the table: Benign.

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Reference-table entries

CCND1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 11:69462910
Cytoband: 11q13.3
HGVS: NM_053056.3(CCND1):c.723G>A (p.Pro241=)
Allele change: Synonymous_P241P

Associated conditions / phenotypes

Colorectal cancer, susceptibility to|VON HIPPEL-LINDAU SYNDROME, MODIFIER OF|Multiple myeloma, translocation 11,14 type

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.