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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CTSF
Single nucleotide variant
(synonymous variant)
not provided
+3 more
GBenign
CTSF
(N378S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance