RS775437084 SPTLC2

Health Risk Chr 14:77576851
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Associated Conditions
Neuropathy
hereditary sensory and autonomic
type 1C
Inborn genetic diseases
Hereditary neuropathy or pain disorder
Neuropathy
hereditary sensory and autonomic
type 1C
Inborn genetic diseases
Hereditary neuropathy or pain disorder
Other Variants in SPTLC2
rs769807904 rs1024879456 rs2079576918 rs752351930 rs2079620247 rs2079675267 rs747168398 rs2140039094 rs2503570171 rs780807321
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