Variant (rsID / SNP)
rs35503235
rs35503235 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DSCAML1. Location: chromosome 11, position 117,392,110. The table records no clinical significance for this variant.
Reference-table entries
DSCAML1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 11:117392110
- HGVS
- NM_020693.4,c.948T>C,p.His316His
- Allele change
- Synonymous_H376H
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
