Gene entry

SLC46A1

solute carrier family 46 member 1

Chromosome: 17
Cytoband: 17q11.2
Variants (rsID): 4

SLC46A1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17q11.2). Its official name is “solute carrier family 46 member 1”. The reference table lists 4 variants (rsID) for this gene.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Clinically classified variants

3 reference-table entries with clinical significance.

rs117451747Benignsingle nucleotide variantCongenital defect of folate absorption
rs118138669Benignsingle nucleotide variantCongenital defect of folate absorption
rs189103810Uncertain significancesingle nucleotide variantCongenital defect of folate absorption

Other listed variants

rs41296467

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.