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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130068621, NDUFA1
Single nucleotide variant
(5 prime UTR variant)
Inborn genetic diseases
+2 more
GBenign
LOC130068621, NDUFA1
(G32R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+4 more
GBenign/Likely benign
NDUFA1
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+2 more
GBenign/Likely benign
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