Variant (rsID / SNP)

rs201434721

rs201434721 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CTSD. Location: chromosome 11, position 1,774,714. Clinical significance in the table: Benign.

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Reference-table entries

CTSDBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 11:1774714
Cytoband: 11p15.5
HGVS: NM_001909.5(CTSD):c.*19G>A
Allele change: Silent

Associated conditions / phenotypes

Neuronal ceroid lipofuscinosis 10

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.