Variant (rsID / SNP)

rs41272114

rs41272114 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LPA. Location: chromosome 6, position 161,006,077. Clinical significance in the table: Benign.

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Reference-table entries

LPABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:161006077
Cytoband: 6q25.3
HGVS: NM_005577.4(LPA):c.4289+1G>A
Allele change: Silent

Associated conditions / phenotypes

Lipoprotein(a) deficiency, congenital

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.