RS1166138315 MYO5B

Health Risk Chr 18:49992427
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Associated Conditions
Congenital microvillous atrophy
Inborn genetic diseases
Congenital microvillous atrophy
Inborn genetic diseases
Other Variants in MYO5B
rs2511324962 rs121908103 rs121908104 rs121908105 rs121908106 rs727505395 rs727505394 rs199588107 rs749018115 rs183991942
Ask Dr. Hemsworth about this variant