Variant (rsID / SNP)
rs794728689
rs794728689 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RET. Location: chromosome 10, position 43,619,159. Clinical significance in the table: Pathogenic.
Reference-table entries
RETPathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- Deletion
- Chromosome / position
- 10:43619159
- Cytoband
- 10q11.21
- HGVS
- NM_020975.6(RET):c.2846del (p.Gly949fs)
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.