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Variant (rsID / SNP)

rs238148

DDX27

rs238148 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DDX27. Location: chromosome 20, position 47,850,182. The table records no clinical significance for this variant.

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Reference-table entries

DDX27Not classified
Variant type
synonymous_variant
Chromosome / position
20:47850182
HGVS
NM_001348187.2,c.1302C>T,p.Phe434Phe
Allele change
Synonymous_F465F

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.