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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GSR, LOC130000170
(F23L)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GSR, LOC130000170
Single nucleotide variant
not provided
GUncertain significance
GSR, LOC130000170
Single nucleotide variant
not provided
GUncertain significance
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