RS267607087 SPTLC1

Health Risk Chr 9:92047261
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What This Variant Does
"CLNSIG=5
Associated Conditions
Neuropathy
hereditary sensory and autonomic
type IA
severe
type 1A
Charcot-Marie-Tooth disease
Hereditary sensory and autonomic neuropathy type 1
Neuropathy
hereditary sensory and autonomic
type IA
severe
Amyotrophic lateral sclerosis 27
juvenile
Neuropathy
hereditary sensory and autonomic
Other Variants in SPTLC1
rs119482081 rs119482083 rs119482082 rs797045071 rs139086093 rs764460003 rs879254294 rs769188151 rs781435924 rs748723735
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