Variant (rsID / SNP)

rs1152888

rs1152888 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IRAK3. Location: chromosome 12, position 66,605,228. The table records no clinical significance for this variant.

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Reference-table entries

IRAK3Not classified

Variant type: missense_variant&splice_region_variant
Chromosome / position: 12:66605228
HGVS: NM_007199.3,c.439A>G,p.Ile147Val
Allele change: Missense_I86V

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.