RS753770252 VPS13B

Health Risk Chr 8:99832510
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Cohen syndrome
Inborn genetic diseases
Cohen syndrome
Other Variants in VPS13B
rs180177327 rs120074149 rs120074150 rs28940272 rs120074151 rs120074152 rs120074153 rs120074154 rs180177329 rs386834054
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