RS121909112 HSPB1

Health Risk Chr 7:76303855
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What This Variant Does
"[OMIM:?]
Associated Conditions
Neuronopathy
distal hereditary motor
type 2B
Charcot-Marie-Tooth disease axonal type 2F
Charcot-Marie-Tooth disease
HSPB1-related axonal neuropathies
Inborn genetic diseases
Neuronopathy
distal hereditary motor
type 2B
Charcot-Marie-Tooth disease axonal type 2F
Charcot-Marie-Tooth disease
HSPB1-related axonal neuropathies
Inborn genetic diseases
Other Variants in HSPB1
rs28939680 rs29001571 rs28937568 rs28937569 rs28939681 rs104894020 rs121909113 rs587781250 rs367857772 rs863225022
Ask Dr. Hemsworth about this variant