Variant (rsID / SNP)

rs4875958

rs4875958 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLN8. Location: chromosome 8, position 1,721,090. The table records no clinical significance for this variant.

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Reference-table entries

CLN8Not classified

Variant type: intron_variant
Chromosome / position: 8:1721090
HGVS: NM_018941.4,c.543+1327G>A
Allele change: Silent

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.