RS587776542 NHLRC1

Health Risk Chr 6:18122138
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What This Variant Does
"CLNSIG=5
Associated Conditions
Myoclonic epilepsy of Lafora 2
Lafora disease
Inborn genetic diseases
Myoclonic epilepsy of Lafora 2
Lafora disease
Inborn genetic diseases
Other Variants in NHLRC1
rs28940575 rs28940576 rs587776543 rs121917875 rs121917876 rs137852859 rs769301934 rs139029314 rs794726964 rs146636139
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