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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126863275, MED12
(R455W)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
LOC126863275, MED12
Single nucleotide variant
(intron variant)
not provided
+2 more
GBenign
LOC126863275, MED12
Single nucleotide variant
(synonymous variant)
Familial thoracic aortic aneurysm and aortic dissection
+3 more
GBenign
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