Variant (rsID / SNP)

rs6808835

rs6808835 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCRL2. Location: chromosome 3, position 46,449,864. The table records no clinical significance for this variant.

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Reference-table entries

CCRL2Not classified

Variant type: synonymous_variant
Chromosome / position: 3:46449864
HGVS: NM_001130910.2,c.330G>T,p.Gly110Gly
Allele change: Synonymous_G98G

Associated conditions / phenotypes

Atherosclerosis Susceptibility

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.