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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHCHD10
Single nucleotide variant
(synonymous variant +1 more)
Autosomal dominant mitochondrial myopathy with exercise intolerance
+3 more
GBenign
CHCHD10
Single nucleotide variant
(intron variant)
Autosomal dominant mitochondrial myopathy with exercise intolerance
+3 more
GBenign
CHCHD10
Single nucleotide variant
(synonymous variant +1 more)
not provided
+5 more
GBenign/Likely benign
CHCHD10
Single nucleotide variant
(synonymous variant)
Autosomal dominant mitochondrial myopathy with exercise intolerance
+3 more
GBenign
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