RS532268197 CDHR1

Health Risk Chr 10:84211133
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Associated Conditions
Inborn genetic diseases
Optic atrophy
Inborn genetic diseases
Optic atrophy
Other Variants in CDHR1
rs781781440 rs747425652 rs763399323 rs786205459 rs786205613 rs794726954 rs794727197 rs190906755 rs878853347 rs137876961
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