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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IFITM5
(S40W)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic/Likely pathogenic
CDC45
(R373W +3 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
CDC45
(N111fs +1 more)
Microsatellite
(frameshift variant +2 more)
Meier-Gorlin syndrome 7
GPathogenic
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