Variant (rsID / SNP)
rs6594664
rs6594664 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MCC. Location: chromosome 5, position 112,384,802. The table records no clinical significance for this variant.
Reference-table entries
MCCNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 5:112384802
- HGVS
- NM_001085377.2,c.2643C>T,p.Asp881Asp
- Allele change
- Synonymous_D691D
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.