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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129934128, MOGS
Single nucleotide variant
(intron variant +1 more)
not specified
+2 more
GConflicting classifications of pathogenicity
LOC129934128, MOGS
(V62M)
Single nucleotide variant
(missense variant +1 more)
not specified
+1 more
GBenign