Variant (rsID / SNP)

rs6449213

rs6449213 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC2A9. Location: chromosome 4, position 9,994,215. Clinical significance in the table: association.

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Reference-table entries

SLC2A9Association

Clinical significance (as recorded): association
Variant type: single nucleotide variant
Chromosome / position: 4:9994215
Cytoband: 4p16.1
HGVS: NM_020041.3(SLC2A9):c.410+4190G>A
Allele change: Silent

Associated conditions / phenotypes

Uric acid concentration, serum, quantitative trait locus 2

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.