Variant (rsID / SNP)
rs35671
rs35671 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SEC13. Location: chromosome 3, position 10,353,626. The table records no clinical significance for this variant.
Reference-table entries
SEC13Not classified
- Variant type
- missense_variant
- Chromosome / position
- 3:10353626
- HGVS
- NM_001278946.2,c.473G>A,p.Arg158His
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.