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Variant (rsID / SNP)

rs34471100

RDX

rs34471100 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RDX. Location: chromosome 11, position 110,104,081. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

RDXConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
11:110104081
Cytoband
11q22.3
HGVS
NM_002906.4(RDX):c.1468G>A (p.Asp490Asn)
Allele change
Missense_D490N

Public references

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