RS760014795 TTPA

Health Risk Chr 8:63086003
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What This Variant Does
"CLNSIG=5
Associated Conditions
Familial isolated deficiency of vitamin E
Inborn genetic diseases
Familial isolated deficiency of vitamin E
Inborn genetic diseases
Other Variants in TTPA
rs397515377 rs121917849 rs397515379 rs121917850 rs121917851 rs397515522 rs143010236 rs397515524 rs1554605631 rs35916840
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