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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
OPTN, LOC108903148
Single nucleotide variant
(synonymous variant)
Primary open angle glaucoma
+4 more
GBenign
OPTN, LOC108903148
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+5 more
GBenign/Likely benign
LOC108903148, OPTN
(M98K)
Single nucleotide variant
(missense variant)
Amyotrophic lateral sclerosis type 12
+5 more
GBenign/Likely benign
OPTN
Single nucleotide variant
(intron variant)
Primary open angle glaucoma
+4 more
GBenign
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