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Variant (rsID / SNP)

rs1129640

DDX39B

rs1129640 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DDX39B. Location: chromosome 6, position 31,506,624. The table records no clinical significance for this variant.

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Reference-table entries

DDX39BNot classified
Variant type
synonymous_variant
Chromosome / position
6:31506624
HGVS
NM_004640.7,c.348A>G,p.Val116Val
Allele change
Synonymous_V116V

Public references

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