Variant (rsID / SNP)
rs775924858
rs775924858 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LDLR. Location: chromosome 19, position 11,224,126. Clinical significance in the table: Pathogenic/Likely pathogenic.
Reference-table entries
LDLRPathogenic
- Clinical significance (as recorded)
- Pathogenic/Likely pathogenic
- Variant type
- single nucleotide variant
- Chromosome / position
- 19:11224126
- Cytoband
- 19p13.2
- HGVS
- NM_000527.5(LDLR):c.1358+1G>A
- Allele change
- Silent
Associated conditions / phenotypes
Hypercholesterolemia, familial, 1
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.