Variant (rsID / SNP)

rs386833968

rs386833968 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLN5. Location: chromosome 13, position 77,575,017. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

CLN5Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 13:77575017
Cytoband: 13q22.3
HGVS: NM_006493.4(CLN5):c.990G>T (p.Trp330Cys)
Allele change: Missense_W379C

Associated conditions / phenotypes

Neuronal ceroid lipofuscinosis 5|Neuronal ceroid lipofuscinosis

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.