Variant (rsID / SNP)
rs5174
rs5174 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRP8. Location: chromosome 1, position 53,712,727. Clinical significance in the table: risk factor.
Reference-table entries
LRP8Risk factor
- Clinical significance (as recorded)
- risk factor
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:53712727
- Cytoband
- 1p32.3
- HGVS
- NM_004631.5(LRP8):c.2855G>A (p.Arg952Gln)
- Allele change
- Missense_R782Q
Associated conditions / phenotypes
Myocardial infarction 1
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.