RS764460003 SPTLC1

Health Risk Chr 9:92108792
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Associated Conditions
Hereditary sensory and autonomic neuropathy type 1
Inborn genetic diseases
Hereditary sensory and autonomic neuropathy type 1
Inborn genetic diseases
Other Variants in SPTLC1
rs119482081 rs119482083 rs119482082 rs267607087 rs797045071 rs139086093 rs879254294 rs769188151 rs781435924 rs748723735
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