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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129998297, SUGCT
(H6Y)
Single nucleotide variant
(5 prime UTR variant)
not specified
+1 more
GUncertain significance
LOC129998297, SUGCT
(A9T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LOC129998297, SUGCT
Single nucleotide variant
(synonymous variant)
not provided
GBenign
LOC129998297, SUGCT
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
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