RS763487608 MYO18B

Health Risk Chr 22:26026799
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Associated Conditions
Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome
Inborn genetic diseases
Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome
Inborn genetic diseases
Other Variants in MYO18B
rs267606197 rs556752387 rs869312740 rs192639023 rs149103381 rs1569308524 rs756408696 rs1569172839 rs35252978 rs201312229
Ask Dr. Hemsworth about this variant