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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GMNN
Single nucleotide variant
(5 prime UTR variant)
GMNN-related disorder
GBenign
GMNN
(N18T)
Single nucleotide variant
(missense variant)
GMNN-related disorder
+1 more
GBenign
GMNN
(S60P)
Single nucleotide variant
(missense variant)
not provided
+1 more
GLikely benign
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