Variant (rsID / SNP)
rs10900296
rs10900296 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RET. Location: chromosome 10, position 43,572,507. Clinical significance in the table: Benign.
Reference-table entries
RETBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 10:43572507
- Cytoband
- 10q11.21
- HGVS
- NM_020630.5(RET):c.-200A>G
- Allele change
- Silent
Associated conditions / phenotypes
Multiple endocrine neoplasia|Hirschsprung Disease, Dominant|Renal hypodysplasia/aplasia 1|Pheochromocytoma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.