RS587782210 SDHD
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary cancer-predisposing syndrome
Paragangliomas with sensorineural hearing loss
Carney-Stratakis syndrome
Pheochromocytoma
Cowden syndrome 3
Hereditary cancer-predisposing syndrome
Paragangliomas with sensorineural hearing loss
Carney-Stratakis syndrome
Pheochromocytoma
Cowden syndrome 3
Other Variants in SDHD