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Variant (rsID / SNP)

rs7306824

CD163L1

rs7306824 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CD163L1. Location: chromosome 12, position 7,528,471. The table records no clinical significance for this variant.

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Reference-table entries

CD163L1Not classified
Variant type
synonymous_variant
Chromosome / position
12:7528471
HGVS
NM_001297650.2,c.2541C>T,p.Asn847Asn
Allele change
Synonymous_N837N

Public references

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