Variant (rsID / SNP)

rs17073322

rs17073322 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KPNA3. Location: chromosome 13, position 50,283,819. The table records no clinical significance for this variant.

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Reference-table entries

KPNA3Not classified

Variant type: synonymous_variant
Chromosome / position: 13:50283819
HGVS: NM_002267.4,c.921A>G,p.Ala307Ala
Allele change: Synonymous_A307A

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.