RS747177622 AFG2B

Health Risk Chr 15:45410399
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Associated Conditions
Hearing loss
autosomal recessive 119
Hearing loss
autosomal recessive 119
Other Variants in AFG2B
rs2140692680 rs148815842 rs747249958 rs765912979 rs763343580 rs778481503 rs1212383243 rs1230836596 rs34675173 rs777812455
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