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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GLS
(G42V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GLS, LOC129935270
(P100L)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GLS
(A114fs)
Duplication
(frameshift variant)
not provided
GLikely pathogenic
GLS
(K289N)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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