Variant (rsID / SNP)

rs2229638

rs2229638 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ITPR3. Location: chromosome 6, position 33,648,228. The table records no clinical significance for this variant.

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Reference-table entries

ITPR3Not classified

Variant type: synonymous_variant
Chromosome / position: 6:33648228
HGVS: NM_002224.4,c.4347C>T,p.Ala1449Ala
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.