Variant (rsID / SNP)
rs7302230
rs7302230 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLSTN3. Location: chromosome 12, position 7,288,432. The table records no clinical significance for this variant.
Reference-table entries
CLSTN3Not classified
- Variant type
- missense_variant
- Chromosome / position
- 12:7288432
- HGVS
- NM_014718.4,c.625A>G,p.Ser209Gly
- Allele change
- Missense_S209G
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.