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Variant (rsID / SNP)

rs7867504

SLC28A3

rs7867504 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC28A3. Location: chromosome 9, position 86,920,236. The table records no clinical significance for this variant.

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Reference-table entries

SLC28A3Not classified
Variant type
synonymous_variant
Chromosome / position
9:86920236
HGVS
NM_001199633.2,c.267A>G,p.Thr89Thr
Allele change
Silent

Associated conditions / phenotypes

Neutropenia|Thrombocytopenia|Toxic Encephalopathy

Public references

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