RS766758560 INSR

Health Risk Chr 19:7152930
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in INSR
rs121913135 rs121913136 rs267607184 rs121913137 rs121913140 rs121913138 rs387906538 rs121913139 rs121913141 rs121913142
Ask Dr. Hemsworth about this variant