Variant (rsID / SNP)

rs1556478

rs1556478 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LIPA. Location: chromosome 10, position 90,983,629. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

LIPABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:90983629
Cytoband: 10q23.31
HGVS: NM_000235.4(LIPA):c.676-42G>A
Allele change: Silent

Associated conditions / phenotypes

Lysosomal acid lipase deficiency

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.