Variant (rsID / SNP)
rs3735964
rs3735964 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LPL. Location: chromosome 8, position 19,824,045. Clinical significance in the table: Benign.
Reference-table entries
LPLBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 8:19824045
- Cytoband
- 8p21.3
- HGVS
- NM_000237.3(LPL):c.*1224C>A
- Allele change
- Missense_F884L
Associated conditions / phenotypes
Hyperlipoproteinemia, type I
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.