Variant (rsID / SNP)
rs886041443
rs886041443 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RET. Location: chromosome 10, position 43,601,845. Clinical significance in the table: Pathogenic.
Reference-table entries
RETPathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- Duplication
- Chromosome / position
- 10:43601845
- Cytoband
- 10q11.21
- HGVS
- NM_020975.6(RET):c.890dup (p.Val298fs)
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.