Variant (rsID / SNP)

rs7843828

rs7843828 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCAR2. Location: chromosome 8, position 22,463,623. The table records no clinical significance for this variant.

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Reference-table entries

CCAR2Not classified

Variant type: synonymous_variant
Chromosome / position: 8:22463623
HGVS: NM_001393997.1,c.84C>T,p.Gly28Gly
Allele change: Synonymous_G28G

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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