RS886037952 PPP1CB
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What This Variant Does
"CLNSIG=5
Associated Conditions
Noonan syndrome-like disorder with loose anagen hair 2
Noonan syndrome
Dandy-Walker syndrome
Inborn genetic diseases
Neurodevelopmental delay
RASopathy
Cardiovascular phenotype
Noonan syndrome-like disorder with loose anagen hair 2
Noonan syndrome
Dandy-Walker syndrome
Inborn genetic diseases
Neurodevelopmental delay
RASopathy
Cardiovascular phenotype
Other Variants in PPP1CB