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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IFT74
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
IFT74, LRRC19
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
IFT74
Single nucleotide variant
(intron variant)
IFT74-related condition
+2 more
GConflicting classifications of pathogenicity
IFT74
(V579M)
Single nucleotide variant
(missense variant +1 more)
not provided
GBenign/Likely benign
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