RS119482083 SPTLC1

Health Risk Chr 9:92068095
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What This Variant Does
"[OMIM:?]
Associated Conditions
Hereditary sensory and autonomic neuropathy type 1
Charcot-Marie-Tooth disease
Neuropathy
hereditary sensory and autonomic
type 1A
Inborn genetic diseases
SPTLC1-related disorder
Hereditary sensory and autonomic neuropathy type 1
Charcot-Marie-Tooth disease
Neuropathy
hereditary sensory and autonomic
type 1A
Inborn genetic diseases
SPTLC1-related disorder
Other Variants in SPTLC1
rs119482081 rs119482082 rs267607087 rs797045071 rs139086093 rs764460003 rs879254294 rs769188151 rs781435924 rs748723735
Ask Dr. Hemsworth about this variant