Variant (rsID / SNP)

rs267607058

rs267607058 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC29A3. Location: chromosome 10, position 73,122,283. Clinical significance in the table: Pathogenic.

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Reference-table entries

SLC29A3Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 10:73122283
Cytoband: 10q22.1
HGVS: NM_018344.6(SLC29A3):c.1346C>G (p.Thr449Arg)
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.