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Variant (rsID / SNP)

rs6558165

CCAR2

rs6558165 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCAR2. Location: chromosome 8, position 22,473,224. The table records no clinical significance for this variant.

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Reference-table entries

CCAR2Not classified
Variant type
synonymous_variant
Chromosome / position
8:22473224
HGVS
NM_001393997.1,c.1407T>C,p.Asp469Asp
Allele change
Synonymous_D469D

Public references

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