Variant (rsID / SNP)
rs10402812
rs10402812 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUC16. Location: chromosome 19, position 9,086,123. The table records no clinical significance for this variant.
Reference-table entries
MUC16Not classified
- Variant type
- missense_variant
- Chromosome / position
- 19:9086123
- HGVS
- NM_001401501.1,c.5812T>G,p.Tyr1938Asp
- Allele change
- Missense_Y1898D
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.