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rs112205661(C;T)

From SNPedia

unaffected carrier of rare mutation
Is agenotype
ofrs112205661
GeneDARS
Chromosome2
Position135,920,590
mentionedby
Magnitude2
Geno Mag Summary
(C;C) 0 common
(C;T) 2 unaffected carrier of rare mutation
(T;T) 5 likely hypomyelination with brainstem and spinal cord involvement and leg spasticity; see discussion