RS142153571 SPTLC1

Health Risk Chr 9:92112500
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Associated Conditions
Hereditary sensory and autonomic neuropathy type 1
Charcot-Marie-Tooth disease
Neuropathy
hereditary sensory and autonomic
type 1A
Inborn genetic diseases
Hereditary sensory and autonomic neuropathy type 1
Charcot-Marie-Tooth disease
Neuropathy
hereditary sensory and autonomic
type 1A
Inborn genetic diseases
Other Variants in SPTLC1
rs119482081 rs119482083 rs119482082 rs267607087 rs797045071 rs139086093 rs764460003 rs879254294 rs769188151 rs781435924
Ask Dr. Hemsworth about this variant