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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC108903148, OPTN
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
OPTN, LOC108903148
(R83C)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
LOC108903148, OPTN
(E92V)
Single nucleotide variant
(missense variant)
Amyotrophic lateral sclerosis
+5 more
GUncertain significance
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