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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WFS1
(A684V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+6 more
GPathogenic
WFS1
(R685C)
Single nucleotide variant
(missense variant)
Monogenic diabetes
+3 more
GConflicting classifications of pathogenicity