Variant (rsID / SNP)
rs1800862
rs1800862 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RET. Location: chromosome 10, position 43,615,094. 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
- 10:43615094
- Cytoband
- 10q11.21
- HGVS
- NM_020975.6(RET):c.2508C>T (p.Ser836_Ser837=)
- Allele change
- Synonymous_S836S
Associated conditions / phenotypes
Multiple endocrine neoplasia|Hirschsprung disease, susceptibility to, 1|Pheochromocytoma|Renal hypodysplasia/aplasia 1|Hereditary cancer-predisposing syndrome|Multiple endocrine neoplasia, type 2
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.