Variant (rsID / SNP)
rs2000813
rs2000813 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LIPG. Location: chromosome 18, position 47,093,864. The table records no clinical significance for this variant.
Reference-table entries
LIPGNot classified
- Variant type
- missense_variant
- Chromosome / position
- 18:47093864
- HGVS
- NM_006033.4,c.332C>T,p.Thr111Ile
- Allele change
- Missense_T111I
Associated conditions / phenotypes
Lipoprotein Quantitative Trait Locus|Arteries, Anomalies of|Body Mass Index Quantitative Trait Locus 1|Microvascular Complications of Diabetes 5|Lipid Metabolism Disorder
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.