RS886037943 SLC1A2

Health Risk Chr 11:35315079
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What This Variant Does
"CLNSIG=5
Associated Conditions
Developmental and epileptic encephalopathy
41
Inborn genetic diseases
Developmental and epileptic encephalopathy
41
Inborn genetic diseases
Other Variants in SLC1A2
rs201446570 rs2497859234 rs892203135 rs766885690 rs371540867 rs1364953579 rs2497830626 rs932831703 rs2497617328 rs2497774921
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