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Variant (rsID / SNP)

rs3094225

CCHCR1

rs3094225 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCHCR1. Location: chromosome 6, position 31,113,052. The table records no clinical significance for this variant.

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Reference-table entries

CCHCR1Not classified
Variant type
synonymous_variant
Chromosome / position
6:31113052
HGVS
NM_001394641.1,c.1794C>T,p.Asp598Asp
Allele change
Synonymous_D553D

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.