Variant (rsID / SNP)

rs116843064

rs116843064 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANGPTL4. Location: chromosome 19, position 8,429,323. Clinical significance in the table: association.

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Reference-table entries

ANGPTL4Association

Clinical significance (as recorded): association
Variant type: single nucleotide variant
Chromosome / position: 19:8429323
Cytoband: 19p13.2
HGVS: NM_139314.3(ANGPTL4):c.118G>A (p.Glu40Lys)
Allele change: Missense_E40K

Associated conditions / phenotypes

Plasma triglyceride level quantitative trait locus

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.