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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FXN, LOC130001862
Single nucleotide variant
(5 prime UTR variant)
not specified
+1 more
GBenign
FXN, LOC130001862
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+3 more
GBenign