Gene entry

SLC25A19

solute carrier family 25 member 19

Chromosome: 17
Cytoband: 17q25.1
Variants (rsID): 8

SLC25A19 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17q25.1). Its official name is “solute carrier family 25 member 19”. The reference table lists 8 variants (rsID) for this gene.

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Clinically classified variants

3 reference-table entries with clinical significance.

rs142281464Benignsingle nucleotide variantAmish lethal microcephaly
rs147904037Conflicting interpretationssingle nucleotide variant
rs148372053Conflicting interpretationssingle nucleotide variantAmish lethal microcephaly

Other listed variants

rs7218042
rs9944529
rs138452752
rs181826033
rs185916833

Public references

NCBI Gene
Ensembl
ClinVar

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.