Variant (rsID / SNP)
rs121913313
rs121913313 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RET. Location: chromosome 10, position 43,609,078. Clinical significance in the table: Likely pathogenic.
Reference-table entries
RETLikely pathogenic
- Clinical significance (as recorded)
- Likely pathogenic
- Variant type
- Deletion
- Chromosome / position
- 10:43609078
- Cytoband
- 10q11.21
- HGVS
- NM_020975.6(RET):c.1834_1860del (p.Phe612_Cys620del)
Associated conditions / phenotypes
Medullary thyroid carcinoma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.