RS869025193 RIT1

Health Risk Chr 1:155904498
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What This Variant Does
"CLNSIG=5
Associated Conditions
Noonan syndrome 8
Noonan syndrome
RASopathy
Inborn genetic diseases
Noonan syndrome and Noonan-related syndrome
RIT1-related disorder
Noonan syndrome 8
Noonan syndrome
RASopathy
Inborn genetic diseases
Noonan syndrome and Noonan-related syndrome
RIT1-related disorder
Other Variants in RIT1
rs672601334 rs672601335 rs483352822 rs730881014 rs730881012 rs869025197 rs869025196 rs869025195 rs869025194 rs869025192
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