RS387906936 TPK1

Health Risk Chr 7:144682975
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What This Variant Does
"CLNSIG=5
Associated Conditions
Childhood encephalopathy due to thiamine pyrophosphokinase deficiency
Inborn genetic diseases
Childhood encephalopathy due to thiamine pyrophosphokinase deficiency
Inborn genetic diseases
Other Variants in TPK1
rs387906935 rs1563989427 rs371271054 rs375169579 rs863224238 rs747753388 rs863224237 rs769525399 rs368458768 rs776874412
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