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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FN1
(P1913L +3 more)
Single nucleotide variant
(missense variant +1 more)
See cases
GLikely pathogenic
FN1
(T278S)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance