Variant (rsID / SNP)

rs4883263

rs4883263 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CD163. Location: chromosome 12, position 7,649,484. The table records no clinical significance for this variant.

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Reference-table entries

CD163Not classified

Variant type: missense_variant
Chromosome / position: 12:7649484
HGVS: NM_004244.6,c.1024A>G,p.Ile342Val
Allele change: Missense_I342V

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.