RS104894129 TPM2

Health Risk Chr 9:35685672
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What This Variant Does
"[OMIM:?]
Associated Conditions
Congenital myopathy 23
Arthrogryposis
distal
type 1A
Inborn genetic diseases
Congenital myopathy 23
Arthrogryposis
distal
type 1A
Inborn genetic diseases
Other Variants in TPM2
rs104894127 rs137853305 rs137853306 rs199476153 rs199476147 rs137853307 rs199476146 rs199476151 rs199476154 rs35401252
Ask Dr. Hemsworth about this variant