Variant (rsID / SNP)

rs9956630

rs9956630 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALPK2. Location: chromosome 18, position 56,247,567. The table records no clinical significance for this variant.

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Reference-table entries

ALPK2Not classified

Variant type: synonymous_variant
Chromosome / position: 18:56247567
HGVS: NM_052947.4,c.441T>C,p.Tyr147Tyr
Allele change: Synonymous_Y147Y

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.