RS587777782 SYT2

Health Risk Chr 1:202599348
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What This Variant Does
"CLNSIG=5
Associated Conditions
Congenital myasthenic syndrome 7
Inborn genetic diseases
Congenital myasthenic syndrome 7
Inborn genetic diseases
Other Variants in SYT2
rs2149068434 rs2526974512 rs142804180 rs1690636110 rs2526989632 rs2526969474 rs1690515734 rs2149066990 rs1690455297 rs752537599
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