Variant (rsID / SNP)
rs114172780
rs114172780 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VLDLR. Location: chromosome 9, position 2,644,829. Clinical significance in the table: Benign/Likely benign.
Reference-table entries
VLDLRBenign
- Clinical significance (as recorded)
- Benign/Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 9:2644829
- Cytoband
- 9p24.2
- HGVS
- NM_003383.5(VLDLR):c.1162C>T (p.Leu388=)
- Allele change
- Synonymous_L388L
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.