Variant (rsID / SNP)

rs7296261

rs7296261 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLSTN3. Location: chromosome 12, position 7,309,199. The table records no clinical significance for this variant.

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Reference-table entries

CLSTN3Not classified

Variant type: intron_variant
Chromosome / position: 12:7309199
HGVS: NM_014718.4,c.2528-886G>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.