Variant (rsID / SNP)

rs1056719

rs1056719 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DAPK1. Location: chromosome 9, position 90,322,023. The table records no clinical significance for this variant.

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Reference-table entries

DAPK1Not classified

Variant type: missense_variant
Chromosome / position: 9:90322023
HGVS: NM_001288729.2,c.4037G>A,p.Ser1346Asn
Allele change: Missense_S1346N

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.