RS786203932 SDHD

Health Risk Chr 11:112094902
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What This Variant Does
"CLNSIG=4
Associated Conditions
Hereditary cancer-predisposing syndrome
Cowden syndrome 3
Pheochromocytoma
Paragangliomas with sensorineural hearing loss
Carney-Stratakis syndrome
Hereditary cancer-predisposing syndrome
Cowden syndrome 3
Pheochromocytoma
Paragangliomas with sensorineural hearing loss
Carney-Stratakis syndrome
Other Variants in SDHD
rs104894303 rs80338843 rs587776644 rs34677591 rs80338844 rs80338845 rs104894302 rs587776645 rs104894304 rs104894305
Ask Dr. Hemsworth about this variant