RS483352822 RIT1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Noonan syndrome 8
Noonan syndrome
Noonan syndrome and Noonan-related syndrome
RASopathy
Noonan syndrome 8
Noonan syndrome and Noonan-related syndrome
RIT1-related disorder
Cardiovascular phenotype
RASopathy
Noonan syndrome 8
Inborn genetic diseases
RASopathy
Noonan syndrome 8
Noonan syndrome
Noonan syndrome and Noonan-related syndrome
Other Variants in RIT1