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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GEMIN7, LOC130064668
+1 more
(I32M)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GEMIN7, LOC130064668
+1 more
(M25L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GEMIN7, LOC130064668
+1 more
(E14Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
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