Variant (rsID / SNP)

rs149276836

rs149276836 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LAMP2. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

LAMP2Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Cytoband: Xq24
HGVS: NM_002294.3(LAMP2):c.385G>A (p.Ala129Thr)
Allele change: Missense_A129T

Associated conditions / phenotypes

Danon disease|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.