Variant (rsID / SNP)
rs1044250
rs1044250 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANGPTL4. Location: chromosome 19, position 8,436,164. The table records no clinical significance for this variant.
Reference-table entries
ANGPTL4Not classified
- Variant type
- missense_variant
- Chromosome / position
- 19:8436164
- HGVS
- NM_139314.3,c.797C>T,p.Thr266Met
- Allele change
- Missense_T266M
Associated conditions / phenotypes
Proteinuria, Chronic Benign|Nephrotic Syndrome|Lipid Metabolism Disorder|Type 2 Diabetes Mellitus|Lipoprotein Quantitative Trait Locus|Arteries, Anomalies of|Arteriovenous Malformation|Plasma Triglyceride Level Quantitative Trait Locus
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.