RS199474673 MT-TW

Health Risk Chr MT:5521
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn mitochondrial myopathy
MELAS syndrome
Mitochondrial disease
Primary mitochondrial disorders
Inborn mitochondrial myopathy
MELAS syndrome
Mitochondrial disease
Primary mitochondrial disorders
Other Variants in MT-TW
rs199474672 rs387906736 rs1603220010
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