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rs121917749(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs121917749
GeneSCN2A
Chromosome2
Position165,374,700
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 4 Benign familial neonatal-infantile seizures