RS267606898 MT-ND5

Health Risk Chr MT:13042
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What This Variant Does
"CLNSIG=5
Associated Conditions
MELAS syndrome
MERRF syndrome
Leigh syndrome due to mitochondrial complex I deficiency
Leber optic atrophy
Mitochondrial disease
Primary mitochondrial disorders
MELAS syndrome
MERRF syndrome
Leigh syndrome due to mitochondrial complex I deficiency
Leber optic atrophy
Mitochondrial disease
Primary mitochondrial disorders
Other Variants in MT-ND5
rs267606893 rs267606897 rs587776440 rs1603223730 rs1603224015 rs1603224029 rs1603224043 rs1603223971
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