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rs387906709(C;C)

From SNPedia

common in clinvar
Is agenotype
ofrs387906709
GeneUBQLN2
ChromosomeX
Position56,565,363
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;A) 7.9 Amyotrophic lateral sclerosis, type 15
(A;C) 7.9 Amyotrophic lateral sclerosis, type 15
(C;C) 0 common in clinvar
(C;T) 7.9 Heterogenous neurodegeneration disorder
(T;T) 7.9 Heterogeneous neurodegeneration disorder