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rs606231128(-;-)

From SNPedia
common in clinvar
Is agenotype
ofrs606231128
GeneDOK7
Chromosome4
Position3,493,113
Merged fromRs764365793
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;-) 0 common in clinvar
(-;TGCC) 3 Carrier of a mutation for congenital myasthenic syndrome
(TGCC;TGCC) 5.5 Congenital myasthenic syndrome, type 10