RS373849532 HINT1

Health Risk Chr 5:131159494
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive axonal neuropathy with neuromyotonia
Autosomal recessive axonal neuropathy with neuromyotonia
Other Variants in HINT1
rs145306016 rs373197800 rs1755286581 rs1048322333 rs768248277 rs1755365079 rs2149654884 rs1289497047 rs2479569695 rs2479570025
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