RS372000714 IGHMBP2

Health Risk Chr 11:68906120
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Charcot-Marie-Tooth disease axonal type 2S
Autosomal recessive distal spinal muscular atrophy 1
Distal spinal muscular atrophy
Peripheral neuropathy
Inborn genetic diseases
Charcot-Marie-Tooth disease axonal type 2S
Autosomal recessive distal spinal muscular atrophy 1
Distal spinal muscular atrophy
Peripheral neuropathy
Inborn genetic diseases
Other Variants in IGHMBP2
rs137852665 rs137852666 rs137852667 rs137852668 rs786205089 rs137852669 rs786205090 rs137852670 rs724159994 rs724159958
Ask Dr. Hemsworth about this variant