RS137852808 CHRNA1

Health Risk Chr 2:174748183 snv missense variant
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What This Variant Does
"[OMIM:?]
Associated Conditions
Congenital myasthenic syndrome 1A
Congenital myasthenic syndrome 1A
Population Frequencies
gnomAD ALL
0%
Other Variants in CHRNA1
rs137852798 rs137852800 rs137852801 rs137852802 rs137852803 rs137852804 rs137852805 rs137852806 rs137852807 rs1477401624
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