RS776737413 BIN1

Health Risk Chr 2:127052356
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Associated Conditions
Myopathy
centronuclear
2
Autosomal dominant nonsyndromic hearing loss 22
Myopathy
centronuclear
2
Autosomal dominant nonsyndromic hearing loss 22
Other Variants in BIN1
rs121909273 rs121909274 rs121909275 rs267606681 rs115938552 rs138047593 rs587783343 rs35535012 rs114833236 rs370911793
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