RS200702600 ASXL1

Health Risk Chr 20:32435795
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What This Variant Does
"CLNSIG=5
Associated Conditions
Bohring-Opitz syndrome
Inborn genetic diseases
Bohring-Opitz syndrome
Inborn genetic diseases
Other Variants in ASXL1
rs387907077 rs373145711 rs750170870 rs387907078 rs1600588199 rs397515401 rs373486603 rs150119795 rs587778064 rs750955319
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