Variant (rsID / SNP)
rs2472737
rs2472737 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RET. Location: chromosome 10, position 43,615,505. Clinical significance in the table: Benign.
Reference-table entries
RETBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 10:43615505
- Cytoband
- 10q11.21
- HGVS
- NM_020975.6(RET):c.2608-24G>A
- Allele change
- Silent
Associated conditions / phenotypes
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.