Variant (rsID / SNP)

rs1057519647

rs1057519647 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LDLR. Location: chromosome 19, position 11,200,057. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

LDLRLikely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 19:11200057
Cytoband: 19p13.2
HGVS: NM_000527.4(LDLR):c.-168A>G
Allele change: Silent

Associated conditions / phenotypes

Hypercholesterolemia, familial, 1

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.