Variant (rsID / SNP)

rs2304075

rs2304075 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC25A48. Location: chromosome 5, position 135,178,124. The table records no clinical significance for this variant.

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Reference-table entries

SLC25A48Not classified

Variant type: synonymous_variant
Chromosome / position: 5:135178124
HGVS: NM_001349336.2,c.66T>C,p.Val22Val
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.