Variant (rsID / SNP)
rs267607137
rs267607137 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRAPPC9. Location: chromosome 8, position 141,370,230. Clinical significance in the table: Pathogenic/Likely pathogenic.
Reference-table entries
TRAPPC9Pathogenic
- Clinical significance (as recorded)
- Pathogenic/Likely pathogenic
- Variant type
- single nucleotide variant
- Chromosome / position
- 8:141370230
- Cytoband
- 8q24.3
- HGVS
- NM_001160372.4(TRAPPC9):c.1414C>T (p.Arg472Ter)
- Allele change
- Nonsense_R463X
Associated conditions / phenotypes
Intellectual disability, autosomal recessive 13
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.