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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TGFB1
(S337T)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign/Likely benign
TGFB1
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
TGFB1
(R296Q)
Single nucleotide variant
(missense variant)
not provided
GConflicting classifications of pathogenicity
TGFB1
Deletion
(intron variant)
not specified
+1 more
GBenign
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