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Variant (rsID / SNP)

rs1139971

CD82

rs1139971 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CD82. Location: chromosome 11, position 44,640,268. The table records no clinical significance for this variant.

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Reference-table entries

CD82Not classified
Variant type
missense_variant
Chromosome / position
11:44640268
HGVS
NM_002231.4,c.721A>G,p.Ile241Val
Allele change
Missense_I216V

Public references

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