RS34677591 SDHD
Upload your DNA to see your genotype for this variant.
What This Variant Does
"rs34677591, also known as c.34G>
Associated Conditions
Cowden syndrome 3
Pheochromocytoma/paraganglioma syndrome 1
Pheochromocytoma
Hereditary cancer-predisposing syndrome
Carney-Stratakis syndrome
Mitochondrial complex 2 deficiency
nuclear type 3
Paragangliomas with sensorineural hearing loss
Hereditary pheochromocytoma and paraganglioma
Cowden syndrome 3
Pheochromocytoma/paraganglioma syndrome 1
Pheochromocytoma
Hereditary cancer-predisposing syndrome
Carney-Stratakis syndrome
Mitochondrial complex 2 deficiency
Other Variants in SDHD