Variant (rsID / SNP)

rs11909217

rs11909217 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LIPI. Location: chromosome 21, position 15,561,623. Clinical significance in the table: Benign.

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Reference-table entries

LIPIBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 21:15561623
Cytoband: 21q11.2
HGVS: NM_001302998.2(LIPI):c.164G>A (p.Cys55Tyr)
Allele change: Missense_C55Y

Associated conditions / phenotypes

Hypertriglyceridemia, familial

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.