Variant (rsID / SNP)
rs495680
rs495680 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STARD13. Location: chromosome 13, position 33,703,656. The table records no clinical significance for this variant.
Reference-table entries
STARD13Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 13:33703656
- HGVS
- NM_178006.4,c.1158A>G,p.Glu386Glu
- Allele change
- Synonymous_E268E
Associated conditions / phenotypes
Synonymous_E378E
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.