RS2079054125 GPHN

Health Risk Chr 14:67122256
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Associated Conditions
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type C
Inborn genetic diseases
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type C
Inborn genetic diseases
Other Variants in GPHN
rs397518420 rs140021399 rs144247888 rs774132595 rs117256383 rs1567108397 rs1595241291 rs529026517 rs2082439915 rs2066910297
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