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Variant (rsID / SNP)

rs1801177

LPL

rs1801177 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LPL. Location: chromosome 8, position 19,805,708. Clinical significance in the table: Benign/Likely benign; other.

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Reference-table entries

LPLBenign
Clinical significance (as recorded)
Benign/Likely benign; other
Variant type
single nucleotide variant
Chromosome / position
8:19805708
Cytoband
8p21.3
HGVS
NM_000237.3(LPL):c.106G>A (p.Asp36Asn)
Allele change
Missense_D36N

Associated conditions / phenotypes

Hyperlipidemia, familial combined, susceptibility to|Coronary heart disease|Hyperlipoproteinemia, type I

Public references

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