Variant (rsID / SNP)
rs1133190
rs1133190 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CKM. Location: chromosome 19, position 45,818,835. The table records no clinical significance for this variant.
Reference-table entries
CKMNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 19:45818835
- HGVS
- NM_001824.5,c.369T>C,p.Pro123Pro
- Allele change
- Synonymous_P123P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.