RS267606849 GP1BA

Health Risk Chr 17:4934224
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What This Variant Does
"CLNSIG=5
Associated Conditions
Bernard-Soulier syndrome
type A1
type A2
autosomal dominant
Bernard Soulier syndrome
Pseudo von Willebrand disease
Nonarteritic anterior ischemic optic neuropathy
susceptibility to
Bernard-Soulier syndrome
type A1
type A2
autosomal dominant
Bernard Soulier syndrome
Pseudo von Willebrand disease
Nonarteritic anterior ischemic optic neuropathy
Other Variants in GP1BA
rs121908061 rs121908062 rs121908063 rs121908064 rs121908065 rs1394634674 rs1555549041 rs1597638300 rs1597638379 rs1597638398
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