rs112205661(C;C)

common

Is a	genotype
of	rs112205661
Gene	DARS
Chromosome	2
Position	135,920,590
mentioned	by

Magnitude

0

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