Variant (rsID / SNP)

rs306547

rs306547 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DDX31. Location: chromosome 9, position 135,470,414. The table records no clinical significance for this variant.

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Reference-table entries

DDX31Not classified

Variant type: missense_variant
Chromosome / position: 9:135470414
HGVS: NM_001322341.2,c.2107A>G,p.Ile703Val
Allele change: Missense_I799V

Associated conditions / phenotypes

Missense_I703V

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.