Variant (rsID / SNP)

rs35519493

rs35519493 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALPK1. Location: chromosome 4, position 113,352,745. The table records no clinical significance for this variant.

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Reference-table entries

ALPK1Not classified

Variant type: missense_variant
Chromosome / position: 4:113352745
HGVS: NM_001102406.2,c.2042G>A,p.Gly681Asp
Allele change: Missense_G603D

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.