Variant (rsID / SNP)

rs197413

rs197413 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DDX20. Location: chromosome 1, position 112,308,972. The table records no clinical significance for this variant.

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Reference-table entries

DDX20Not classified

Variant type: synonymous_variant
Chromosome / position: 1:112308972
HGVS: NM_007204.5,c.1926G>A,p.Val642Val
Allele change: Synonymous_V642V

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.