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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC108903148, OPTN
(M98K)
Single nucleotide variant
(missense variant)
not specified
+5 more
GBenign/Likely benign
OPTN
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+5 more
GBenign/Likely benign