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Variant (rsID / SNP)

rs4909945

IRAG1

rs4909945 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IRAG1. Location: chromosome 11, position 10,673,739. The table records no clinical significance for this variant.

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Reference-table entries

IRAG1Not classified
Variant type
missense_variant
Chromosome / position
11:10673739
HGVS
NM_001098579.3,c.31A>G,p.Ile11Val
Allele change
Missense_I11V

Public references

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