RS200071478 TNFRSF11B

Health Risk Chr 8:118933105
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Hyperphosphatasemia with bone disease
Hyperphosphatasemia with bone disease
Other Variants in TNFRSF11B
rs796051868 rs104894091 rs2129878039 rs786205594 rs4876870 rs146450643 rs144654126 rs143414212 rs1307942060 rs373848556
Ask Dr. Hemsworth about this variant