RS151266052 SDHA

Health Risk Chr 5:240448
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What This Variant Does
"CLNSIG=5
Associated Conditions
Mitochondrial complex II deficiency
nuclear type 1
Pheochromocytoma/paraganglioma syndrome 5
Hereditary cancer-predisposing syndrome
Hereditary pheochromocytoma and paraganglioma
Gastrointestinal stromal tumor
Mitochondrial complex II deficiency
nuclear type 1
Pheochromocytoma/paraganglioma syndrome 5
Hereditary cancer-predisposing syndrome
Hereditary pheochromocytoma and paraganglioma
Gastrointestinal stromal tumor
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Succinic acid/Methylmalonic acid levels T OR: 1.02 4E-11 PubMed
Other Variants in SDHA
rs9809219 rs137852767 rs1061517 rs137852768 rs387906780 rs142849100 rs587781720 rs587781729 rs80207011 rs587782076
Ask Dr. Hemsworth about this variant