Variant (rsID / SNP)
rs766518430
rs766518430 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GCDH. Location: chromosome 19, position 13,007,152. Clinical significance in the table: Pathogenic/Likely pathogenic.
Reference-table entries
GCDHPathogenic
- Clinical significance (as recorded)
- Pathogenic/Likely pathogenic
- Variant type
- single nucleotide variant
- Chromosome / position
- 19:13007152
- Cytoband
- 19p13.13
- HGVS
- NM_000159.4(GCDH):c.769C>T (p.Arg257Trp)
- Allele change
- Silent
Associated conditions / phenotypes
Glutaric aciduria, type 1
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.