RS137852736 RETREG1

Health Risk Chr 5:16616953
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What This Variant Does
"[OMIM:?]
Associated Conditions
Charcot-Marie-Tooth disease
Neuropathy
hereditary sensory and autonomic
type 2B
Inborn genetic diseases
Hereditary sensory and autonomic neuropathy type 2
Charcot-Marie-Tooth disease
Neuropathy
hereditary sensory and autonomic
type 2B
Inborn genetic diseases
Hereditary sensory and autonomic neuropathy type 2
Other Variants in RETREG1
rs137852739 rs137852737 rs137852738 rs767329180 rs886037748 rs886043753 rs746380834 rs750740230 rs200156015 rs539315640
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