Variant (rsID / SNP)
rs7848919
rs7848919 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GLDC. Location: chromosome 9, position 6,532,477. Clinical significance in the table: Benign.
Reference-table entries
GLDCBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 9:6532477
- Cytoband
- 9p24.1
- HGVS
- NM_000170.3(GLDC):c.*540C>T
- Allele change
- Silent
Associated conditions / phenotypes
Non-ketotic hyperglycinemia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.