Variant (rsID / SNP)
rs374620036
rs374620036 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRCA2. Location: chromosome 13, position 32,914,477. Clinical significance in the table: Likely benign.
Reference-table entries
BRCA2Likely benign
- Clinical significance (as recorded)
- Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 13:32914477
- Cytoband
- 13q13.1
- HGVS
- NM_000059.4(BRCA2):c.5985C>T (p.Asn1995=)
- Allele change
- Synonymous_N1995N
Associated conditions / phenotypes
Hereditary cancer-predisposing syndrome|Breast-ovarian cancer, familial, susceptibility to, 2|Familial cancer of breast|Breast and/or ovarian cancer|Hereditary breast ovarian cancer syndrome|Malignant tumor of breast
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.