Variant (rsID / SNP)

rs397516751

rs397516751 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LAMP2. Clinical significance in the table: Pathogenic.

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Reference-table entries

LAMP2Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: Deletion
Cytoband: Xq24
HGVS: NM_002294.3(LAMP2):c.864+3_864+6del

Associated conditions / phenotypes

Danon disease|Hypertrophic cardiomyopathy

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.