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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CGB3
(D137G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CGB3
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
CGB3
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
CGB3
(R30H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CGB3
(F4L)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
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