Variant (rsID / SNP)

rs4656926

rs4656926 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CD48. Location: chromosome 1, position 160,650,913. The table records no clinical significance for this variant.

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Reference-table entries

CD48Not classified

Variant type: missense_variant
Chromosome / position: 1:160650913
HGVS: NM_001256030.2,c.731T>C,p.Ile244Thr
Allele change: Silent

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.