RS137852803 CHRNA1
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What This Variant Does
"[OMIM:?]
Associated Conditions
Congenital myasthenic syndrome 1A
Inborn genetic diseases
Lethal multiple pterygium syndrome
Myasthenic syndrome
congenital
1B
fast-channel
Congenital myasthenic syndrome 1A
Inborn genetic diseases
Lethal multiple pterygium syndrome
Myasthenic syndrome
congenital
1B
fast-channel
Other Variants in CHRNA1