Variant (rsID / SNP)

rs3210140

rs3210140 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CD163. Location: chromosome 12, position 7,655,137. The table records no clinical significance for this variant.

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Reference-table entries

CD163Not classified

Variant type: synonymous_variant
Chromosome / position: 12:7655137
HGVS: NM_004244.6,c.70T>C,p.Leu24Leu
Allele change: Synonymous_L24L

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.