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Variant (rsID / SNP)

rs1467558

CD44

rs1467558 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CD44. Location: chromosome 11, position 35,229,673. The table records no clinical significance for this variant.

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Reference-table entries

CD44Not classified
Variant type
missense_variant
Chromosome / position
11:35229673
HGVS
NM_000610.4,c.1436T>C,p.Ile479Thr
Allele change
Missense_I230T

Associated conditions / phenotypes

Infantile Liver Failure Syndrome 1|Acute Liver Failure

Public references

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