Variant (rsID / SNP)

rs746408350

rs746408350 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC29A3. Location: chromosome 10, position 73,082,584. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

SLC29A3Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 10:73082584
Cytoband: 10q22.1
HGVS: NM_018344.6(SLC29A3):c.73C>T (p.Arg25Ter)
Allele change: Silent

Associated conditions / phenotypes

H syndrome

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.