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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MED12
(L675F)
Single nucleotide variant
(missense variant)
Wilms tumor 1
+4 more
GUncertain significance
MED12
(K1674del)
Microsatellite
(inframe_deletion)
FG syndrome 1
+2 more
GUncertain significance