Variant (rsID / SNP)
rs117206975
rs117206975 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRAPPC9. Location: chromosome 8, position 141,468,370. Clinical significance in the table: Benign/Likely benign.
Reference-table entries
TRAPPC9Benign
- Clinical significance (as recorded)
- Benign/Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 8:141468370
- Cytoband
- 8q24.3
- HGVS
- NM_031466.8(TRAPPC9):c.-11+10G>A
- Allele change
- Silent
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.