Variant (rsID / SNP)

rs3826593

rs3826593 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALPK2. Location: chromosome 18, position 56,204,747. The table records no clinical significance for this variant.

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Reference-table entries

ALPK2Not classified

Variant type: missense_variant
Chromosome / position: 18:56204747
HGVS: NM_052947.4,c.2672C>T,p.Thr891Ile
Allele change: Missense_T891I

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.