Gene entry
SLC2A9
solute carrier family 2 member 9
- Chromosome
- 4
- Cytoband
- 4p16.1
- Variants (rsID)
- 102
SLC2A9 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 4 (region 4p16.1). Its official name is “solute carrier family 2 member 9”. The reference table lists 102 variants (rsID) for this gene.
Clinically classified variants
7 reference-table entries with clinical significance.
- rs6449213Associationsingle nucleotide variantUric acid concentration, serum, quantitative trait locus 2
- rs737267Associationsingle nucleotide variantUric acid concentration, serum, quantitative trait locus 2
- rs7442295Associationsingle nucleotide variantUric acid concentration, serum, quantitative trait locus 2
- rs116742917Benignsingle nucleotide variantHypouricemia, renal, 2
- rs13125646Benignsingle nucleotide variantHypouricemia, renal, 2
- rs3733591Benignsingle nucleotide variantHypouricemia, renal, 2
- rs121908322Conflicting interpretationssingle nucleotide variantHypouricemia, renal, 2
Other listed variants
- rs4144
- rs734553
- rs938554
- rs1122141
- rs2139242
- rs2176644
- rs2240723
- rs2280333
- rs3756233
- rs3775948
- rs3796840
- rs4336225
- rs4389579
- rs4475146
- rs4481233
- rs4481234
- rs4519796
- rs4529048
- rs4547795
- rs4591605
- rs4639073
- rs4697701
- rs4697909
- rs6449144
- rs6825187
- rs6827401
- rs6832439
- rs6834978
- rs6837273
- rs6838021
- rs6847887
- rs6855911
- rs7657096
- rs7666545
- rs7669607
- rs7678012
- rs7678287
- rs7680126
- rs7683856
- rs7696092
- rs7696983
- rs7698858
- rs9990954
- rs9991278
- rs9998811
- rs10805342
- rs10939558
- rs10939605
- rs11722228
- rs11941148
- rs11942223
- rs12500086
- rs12509955
- rs13101683
- rs13106991
- rs13111638
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.