Variant (rsID / SNP)

rs17683807

rs17683807 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC5A1. Location: chromosome 22, position 32,508,004. Clinical significance in the table: Benign.

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Reference-table entries

SLC5A1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 22:32508004
Cytoband: 22q12.3
HGVS: NM_000343.4(SLC5A1):c.*1804T>C
Allele change: Silent

Associated conditions / phenotypes

Congenital glucose-galactose malabsorption

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.