Variant (rsID / SNP)
rs113660545
rs113660545 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COG5. Location: chromosome 7, position 107,194,758. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
COG5Conflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:107194758
- Cytoband
- 7q22.3
- HGVS
- NM_006348.5(COG5):c.264A>G (p.Ala88=)
- Allele change
- Synonymous_A119A
Associated conditions / phenotypes
COG5-congenital disorder of glycosylation
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.