Variant (rsID / SNP)
rs1596797
rs1596797 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUC16. Location: chromosome 19, position 9,088,017. The table records no clinical significance for this variant.
Reference-table entries
MUC16Not classified
- Variant type
- missense_variant
- Chromosome / position
- 19:9088017
- HGVS
- NM_001401501.1,c.3918A>C,p.Lys1306Asn
- Allele change
- Missense_K1266N
Associated conditions / phenotypes
Ovarian Cancer|Ovarian Epithelial Cancer
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.