RS763428520 STX1B

Health Risk Chr 16:30992843
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What This Variant Does
"CLNSIG=4
Associated Conditions
Generalized epilepsy with febrile seizures plus
type 9
Inborn genetic diseases
STX1B-related disorder
Generalized epilepsy with febrile seizures plus
type 9
Inborn genetic diseases
STX1B-related disorder
Other Variants in STX1B
rs724159973 rs200979563 rs724159974 rs727502806 rs886041666 rs1555493906 rs1555494259 rs758008534 rs1555494222 rs1567379671
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