Variant (rsID / SNP)

rs3134296

rs3134296 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC25A32, DCAF13. Location: chromosome 8, position 104,427,541. The table records no clinical significance for this variant.

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Reference-table entries

SLC25A32Not classified

Variant type: upstream_gene_variant
Chromosome / position: 8:104427541
HGVS: NM_030780.5,c.-376G>A
Allele change: Silent

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.