RS869312963 SBF2

Health Risk Chr 11:9816961
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Charcot-Marie-Tooth disease type 4
Inborn genetic diseases
Charcot-Marie-Tooth disease type 4
Other Variants in SBF2
rs120074137 rs120074138 rs120074139 rs141330687 rs572571832 rs146230559 rs145351367 rs199894823 rs869312970 rs876661288
Ask Dr. Hemsworth about this variant