RS587776691 PMP22

Health Risk Chr 17:15260708
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary liability to pressure palsies
Charcot-Marie-Tooth disease
Hereditary liability to pressure palsies
Charcot-Marie-Tooth disease
Other Variants in PMP22
rs104894617 rs104894618 rs104894619 rs104894620 rs104894621 rs104894622 rs104894623 rs80338763 rs786205087 rs104894624
Ask Dr. Hemsworth about this variant