Variant (rsID / SNP)
rs61737003
rs61737003 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IDH2. Location: chromosome 15, position 90,628,591. Clinical significance in the table: Benign/Likely benign.
Reference-table entries
IDH2Benign
- Clinical significance (as recorded)
- Benign/Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 15:90628591
- Cytoband
- 15q26.1
- HGVS
- NM_002168.4(IDH2):c.996C>T (p.Ser332=)
- Allele change
- Synonymous_S332S
Associated conditions / phenotypes
D-2-hydroxyglutaric aciduria 2
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.