SLC2A9

solute carrier family 2 member 9
OMIM: 606142
PanelMode of inheritanceDetails
3 panels
R-numbers: R256
Signed-off version 2.2
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Hypouricemia, renal, 2, 612076
R-numbers: R198
Signed-off version 2.23
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Hypouricemia, renal, 2, 612076, {Uric acid concentration, serum, QTL 2}, 612076
R-numbers: R257
Signed-off version 1.2
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
{Uric acid concentration, serum, QTL 2}, 612076, Hypouricemia, renal, 2, 612076