Variant (rsID / SNP)
rs1042126
rs1042126 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDSN. Location: chromosome 6, position 31,084,288. The table records no clinical significance for this variant.
Reference-table entries
CDSNNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 6:31084288
- HGVS
- NM_001264.5,c.1104A>G,p.Ala368Ala
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.