Variant (rsID / SNP)

rs63751297

rs63751297 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ASPA. Location: chromosome 17, position 3,386,791. Clinical significance in the table: Pathogenic.

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Reference-table entries

ASPAPathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 17:3386791
Cytoband: 17p13.2
HGVS: NM_000049.4(ASPA):c.433-2A>G
Allele change: Silent

Associated conditions / phenotypes

Canavan Disease, Familial Form

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.