Variant (rsID / SNP)
rs34734558
rs34734558 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MTTP. Location: chromosome 4, position 100,530,143. Clinical significance in the table: Benign.
Reference-table entries
MTTPBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 4:100530143
- Cytoband
- 4q23
- HGVS
- NM_001386140.1(MTTP):c.1769+9C>T
- Allele change
- Silent
Associated conditions / phenotypes
Abetalipoproteinaemia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.