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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126863275, MED12
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+3 more
GBenign
LOC126863275, MED12
Single nucleotide variant
(synonymous variant)
FG syndrome
+1 more
GConflicting classifications of pathogenicity