RS149782619 HINT1

Health Risk Chr 5:131165096
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive axonal neuropathy with neuromyotonia
Peripheral neuropathy
Inborn genetic diseases
Autosomal recessive axonal neuropathy with neuromyotonia
Peripheral neuropathy
Inborn genetic diseases
Other Variants in HINT1
rs145306016 rs373197800 rs1755286581 rs1048322333 rs768248277 rs1755365079 rs2149654884 rs1289497047 rs2479569695 rs2479570025
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