RS369803886 SPTLC1

Health Risk Chr 9:92038334
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Associated Conditions
Hereditary sensory and autonomic neuropathy type 1
Charcot-Marie-Tooth disease
Inborn genetic diseases
Hereditary sensory and autonomic neuropathy type 1
Charcot-Marie-Tooth disease
Inborn genetic diseases
Other Variants in SPTLC1
rs119482081 rs119482083 rs119482082 rs267607087 rs797045071 rs139086093 rs764460003 rs879254294 rs769188151 rs781435924
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