RS119482081 SPTLC1

Health Risk Chr 9:92080045
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What This Variant Does
"rs119482081, also known as c.398G&gt
Associated Conditions
Hereditary sensory and autonomic neuropathy type 1
Neuropathy
hereditary sensory and autonomic
type 1A
Charcot-Marie-Tooth disease
Inborn genetic diseases
Hereditary sensory and autonomic neuropathy type 1
Hereditary sensory and autonomic neuropathy type 1
Neuropathy
hereditary sensory and autonomic
type 1A
Charcot-Marie-Tooth disease
Inborn genetic diseases
Hereditary sensory and autonomic neuropathy type 1
Other Variants in SPTLC1
rs119482083 rs119482082 rs267607087 rs797045071 rs139086093 rs764460003 rs879254294 rs769188151 rs781435924 rs748723735
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