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rs387907313

From SNPedia

ClinVar
Risk rs387907313(T;T)
Alt rs387907313(T;T)
Reference rs387907313(C;C)
Significance Other
Disease Epilepsy not provided
Variation info
Gene SLC2A1
CLNDBN Epilepsy, idiopathic generalized, susceptibility to, 12 not provided
Reversed 1
HGVS NC_000001.10:g.43395437G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000030841.2, RCV000189356.1,