Gene entry

SLC5A5

solute carrier family 5 member 5

Chromosome: 19
Cytoband: 19p13.11
Variants (rsID): 10

SLC5A5 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 19 (region 19p13.11). Its official name is “solute carrier family 5 member 5”. The reference table lists 10 variants (rsID) for this gene.

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Clinically classified variants

3 reference-table entries with clinical significance.

rs45602038Likely benignsingle nucleotide variantFamilial thyroid dyshormonogenesis 1
rs121909180Pathogenicsingle nucleotide variantFamilial thyroid dyshormonogenesis 1|Congenital hypothyroidism
rs121909176Uncertain significancesingle nucleotide variantFamilial thyroid dyshormonogenesis 1

Other listed variants

rs10417391
rs11672428
rs73022605
rs76301117
rs79893861
rs142014480
rs200597118

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.