RS869025195 RIT1

Health Risk Chr 1:155904493
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What This Variant Does
"CLNSIG=5
Associated Conditions
Noonan syndrome
Inborn genetic diseases
Noonan syndrome 1
RASopathy
Noonan syndrome 8
Noonan syndrome
Inborn genetic diseases
Noonan syndrome 1
RASopathy
Noonan syndrome 8
Other Variants in RIT1
rs672601334 rs672601335 rs483352822 rs730881014 rs730881012 rs869025197 rs869025196 rs869025194 rs869025193 rs869025192
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