RS864309522 SLC2A1

Health Risk Chr 1:42927212
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary cryohydrocytosis with reduced stomatin
Inborn genetic diseases
Encephalopathy due to GLUT1 deficiency
Hereditary cryohydrocytosis with reduced stomatin
Inborn genetic diseases
Encephalopathy due to GLUT1 deficiency
Other Variants in SLC2A1
rs80359829 rs80359828 rs80359816 rs80359814 rs2124448824 rs121909739 rs121909740 rs80359812 rs267607060 rs267607061
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