Variant (rsID / SNP)
rs7779633
rs7779633 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STK31. Location: chromosome 7, position 23,751,736. The table records no clinical significance for this variant.
Reference-table entries
STK31Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 7:23751736
- HGVS
- NM_031414.5,c.69A>G,p.Gln23Gln
- Allele change
- Synonymous_Q23Q
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.