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Variant (rsID / SNP)

rs1130146

DDX27

rs1130146 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DDX27. Location: chromosome 20, position 47,859,217. The table records no clinical significance for this variant.

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Reference-table entries

DDX27Not classified
Variant type
missense_variant&splice_region_variant
Chromosome / position
20:47859217
HGVS
NM_001348187.2,c.2296G>A,p.Gly766Ser
Allele change
Missense_G797S

Public references

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