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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MED13
(E1650K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MED13
(S1548G)
Single nucleotide variant
(missense variant)
not specified
+1 more
GBenign