Variant (rsID / SNP)
rs35118262
rs35118262 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RET. Location: chromosome 10, position 43,600,607. Clinical significance in the table: Benign/Likely benign.
Reference-table entries
RETBenign
- Clinical significance (as recorded)
- Benign/Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 10:43600607
- Cytoband
- 10q11.21
- HGVS
- NM_020975.6(RET):c.833C>A (p.Thr278Asn)
- Allele change
- Missense_T278N
Associated conditions / phenotypes
Hereditary cancer-predisposing syndrome|Hirschsprung disease, susceptibility to, 1|Multiple endocrine neoplasia, type 2a|Multiple endocrine neoplasia, type 2|Pheochromocytoma|Multiple endocrine neoplasia|Renal hypodysplasia/aplasia 1
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.