Variant (rsID / SNP)

rs757406292

rs757406292 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to POLD1. Location: chromosome 19, position 50,919,020. Clinical significance in the table: Likely benign.

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Reference-table entries

POLD1Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 19:50919020
Cytoband: 19q13.33
HGVS: NM_002691.4(POLD1):c.2757C>T (p.Gly919=)
Allele change: Synonymous_G919G

Associated conditions / phenotypes

Colorectal cancer, susceptibility to, 10|Hereditary cancer-predisposing 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.