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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHCHD10
(P80L)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+6 more
GConflicting classifications of pathogenicity
CHCHD10
(P34S)
Single nucleotide variant
(missense variant +1 more)
not provided
+5 more
GBenign/Likely benign
CHCHD10
(P16S)
Single nucleotide variant
(missense variant)
Lower motor neuron syndrome with late-adult onset
+2 more
GUncertain significance
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