Variant (rsID / SNP)
rs35296353
rs35296353 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STK33. Location: chromosome 11, position 8,414,229. The table records no clinical significance for this variant.
Reference-table entries
STK33Not classified
- Variant type
- missense_variant
- Chromosome / position
- 11:8414229
- HGVS
- NM_001289061.2,c.1373C>A,p.Ala458Glu
- Allele change
- Missense_A458E
Associated conditions / phenotypes
Missense_A458E|Missense_A458E|Missense_A458E|Missense_A417E|Missense_A458E|Missense_A271E|Missense_A458E|Missense_A417E|Missense_A458E
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.