Variant (rsID / SNP)
rs704219
rs704219 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ST8SIA1. Location: chromosome 12, position 22,354,921. The table records no clinical significance for this variant.
Reference-table entries
ST8SIA1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 12:22354921
- HGVS
- NM_003034.4,c.636T>C,p.Ile212Ile
- Allele change
- Synonymous_I212I
Associated conditions / phenotypes
Demyelinating Disease
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.