Variant (rsID / SNP)
rs76262710
rs76262710 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RET. Location: chromosome 10, position 43,609,096. Clinical significance in the table: Pathogenic.
Reference-table entries
RETPathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- single nucleotide variant
- Chromosome / position
- 10:43609096
- Cytoband
- 10q11.21
- HGVS
- NM_020975.6(RET):c.1852T>G (p.Cys618Gly)
- Allele change
- Missense_C618G
Associated conditions / phenotypes
Multiple endocrine neoplasia, type 2a|Multiple endocrine neoplasia, type 2|6 conditions
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.