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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ABCC6
(V687M +1 more)
Single nucleotide variant
(missense variant +1 more)
Arterial calcification, generalized, of infancy, 2
+4 more
GUncertain significance
ABCC6
(M242I +1 more)
Single nucleotide variant
(missense variant +1 more)
Stroke disorder
GUncertain significance