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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TMEM43
(K168N)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+4 more
GBenign
TMEM43
(M179T)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+4 more
GBenign