RS797044806 XYLT2

Health Risk Chr 17:50354465
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What This Variant Does
"CLNSIG=5
Associated Conditions
Spondylo-ocular syndrome
Inborn genetic diseases
Spondylo-ocular syndrome
Inborn genetic diseases
Other Variants in XYLT2
rs762208911 rs144474638 rs571962145 rs750349082 rs778642140 rs140443495 rs2543952851 rs1912636978 rs2543964027 rs377456488
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