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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130009747, SUCLA2
(R17G)
Single nucleotide variant
(missense variant)
SUCLA2-related condition
+2 more
GConflicting classifications of pathogenicity
SUCLA2, LOC130009747
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign