Variant (rsID / SNP)
rs130073
rs130073 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCHCR1. Location: chromosome 6, position 31,111,180. The table records no clinical significance for this variant.
Reference-table entries
CCHCR1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 6:31111180
- HGVS
- NM_001394641.1,c.2205A>G,p.Leu735Leu
- Allele change
- Synonymous_L690L
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.