Primary hyperoxaluria

At a minimum, these SNPs are known to be related, and others may also be

	Max Magnitude
rs1057516292	0
rs1057516299	0
rs1057516823	0
rs1057516831	0
rs1057516896	0
rs1057516941	0
rs1057516990	0
rs1057517026	0
rs1057517216	0
rs1057517238	0
rs1057517333	0
rs1057517398	0
rs111742810	0
rs111996685	0
rs113681235	0
rs119490108	0
rs121908520	0
rs121908521	0
rs121908522	0
rs121908523	0
rs121908524	0
rs121908525	0
rs121908526	0
rs121908527	0
rs121908528	0
rs121908529	0
rs121908530	0
rs138025751	0
rs138207257	0
rs138584408	0
rs146525143	0
rs149150736	0
rs150702945	0
rs180177155	0
rs180177156	0
rs180177157	0
rs180177158	0
rs180177160	0
rs180177161	0
rs180177162	0
rs180177163	0
rs180177164	0
rs180177165	0
rs180177166	0
rs180177168	0
rs180177170	0
rs180177171	0
rs180177172	0
rs180177173	0
rs180177177	0
... further results

Primary hyperoxaluria of all types is characterized by kidney stones and kidney damage due to a buildup of calcium oxalate deposits. Defects in the glyoxylate reductase/hydroxypyruvate reductase GRHPR gene, inherited as an autosomal recessive condition, are the genetic cause of this disorder.