Variant (rsID / SNP)
rs56195026
rs56195026 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RET. Location: chromosome 10, position 43,615,109. 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
- 10:43615109
- Cytoband
- 10q11.21
- HGVS
- NM_020975.6(RET):c.2523G>A (p.Pro841_Asp842=)
- Allele change
- Synonymous_P841P
Associated conditions / phenotypes
Multiple endocrine neoplasia, type 2|Hereditary cancer-predisposing syndrome|Multiple endocrine neoplasia, type 2a
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.