Variant (rsID / SNP)

rs1134921

rs1134921 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GAK. Location: chromosome 4, position 843,508. The table records no clinical significance for this variant.

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Reference-table entries

GAKNot classified

Variant type: missense_variant
Chromosome / position: 4:843508
HGVS: NM_005255.4,c.3889G>A,p.Asp1297Asn
Allele change: Missense_D1297N

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.