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Variant (rsID / SNP)

rs3741367

CD248

rs3741367 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CD248. Location: chromosome 11, position 66,083,129. The table records no clinical significance for this variant.

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Reference-table entries

CD248Not classified
Variant type
missense_variant
Chromosome / position
11:66083129
HGVS
NM_020404.3,c.1370A>G,p.His457Arg
Allele change
Missense_H457R

Public references

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