RS1339768860 SYN1

Health Risk Chr X:47619358
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Associated Conditions
Inborn genetic diseases
Epilepsy
X-linked 1
with variable learning disabilities and behavior disorders
Inborn genetic diseases
Epilepsy
X-linked 1
with variable learning disabilities and behavior disorders
Other Variants in SYN1
rs137852560 rs397514679 rs200533370 rs150248483 rs587781185 rs794726957 rs375440874 rs794727076 rs775858141 rs372445055
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