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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129934128, MOGS
Single nucleotide variant
(synonymous variant +1 more)
MOGS-related disorder
+1 more
GLikely benign
LOC129934128, MOGS
(R29G)
Single nucleotide variant
(missense variant +1 more)
not specified
+3 more
GBenign/Likely benign