Variant (rsID / SNP)
rs201992974
rs201992974 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RET. Location: chromosome 10, position 43,604,510. Clinical significance in the table: Likely benign.
Reference-table entries
RETLikely benign
- Clinical significance (as recorded)
- Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 10:43604510
- Cytoband
- 10q11.21
- HGVS
- NM_020975.6(RET):c.1095G>A (p.Ser365_Glu366=)
- Allele change
- Synonymous_S365S
Associated conditions / phenotypes
Multiple endocrine neoplasia, type 2|Multiple endocrine neoplasia, type 2b|Multiple endocrine neoplasia, type 2a|Hereditary cancer-predisposing syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.