Variant (rsID / SNP)
rs1446464
rs1446464 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STK33. Location: chromosome 11, position 8,486,310. The table records no clinical significance for this variant.
Reference-table entries
STK33Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 11:8486310
- HGVS
- NM_001289061.2,c.399G>T,p.Ala133Ala
- Allele change
- Synonymous_A133A
Associated conditions / phenotypes
Synonymous_A133A|Synonymous_A133A|Synonymous_A133A|Synonymous_A92A|Synonymous_A133A|Silent|Synonymous_A133A|Synonymous_A92A|Synonymous_A133A|Synonymous_A92A|Synonymous_A92A|Synonymous_A92A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.