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Variant (rsID / SNP)

rs150546732

SLC5A2

rs150546732 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC5A2. Location: chromosome 16, position 31,500,217. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

SLC5A2Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
16:31500217
Cytoband
16p11.2
HGVS
NM_003041.4(SLC5A2):c.1297A>G (p.Ile433Val)
Allele change
Missense_I433V

Associated conditions / phenotypes

Familial renal glucosuria

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.