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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COG1, LOC126862634
(T350M)
Single nucleotide variant
(missense variant)
COG1-related condition
+3 more
GBenign/Likely benign
COG1, LOC126862634
(N392S)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign