RS74315408 PRNP
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What This Variant Does
"[OMIM:?]
Associated Conditions
Inherited Creutzfeldt-Jakob disease
Inherited prion disease
Huntington disease-like 1
6 conditions
Congenital portosystemic shunt
Spongiform encephalopathy with neuropsychiatric features
Inherited Creutzfeldt-Jakob disease
Inherited prion disease
Huntington disease-like 1
6 conditions
Congenital portosystemic shunt
Spongiform encephalopathy with neuropsychiatric features
Other Variants in PRNP