RS1060501915 MFN2

Health Risk Chr 1:11998842
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What This Variant Does
"CLNSIG=5
Associated Conditions
Charcot-Marie-Tooth disease type 2
Inborn genetic diseases
Charcot-Marie-Tooth disease type 2
Inborn genetic diseases
Other Variants in MFN2
rs28940291 rs28940292 rs28940293 rs28940294 rs28940295 rs28940296 rs119103261 rs119103262 rs119103263 rs119103264
Ask Dr. Hemsworth about this variant