RS756880678 LRSAM1

Health Risk Chr 9:127501009
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What This Variant Does
"CLNSIG=5
Associated Conditions
Charcot-Marie-Tooth disease
Charcot-Marie-Tooth disease axonal type 2P
Inborn genetic diseases
Charcot-Marie-Tooth disease
Charcot-Marie-Tooth disease axonal type 2P
Inborn genetic diseases
Other Variants in LRSAM1
rs387907032 rs786200930 rs1564287793 rs200595164 rs797044913 rs876661208 rs876661247 rs138226428 rs201284198 rs879253755
Ask Dr. Hemsworth about this variant