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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FAM111B
(Y489H +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
FAM111B
(F599C +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic
FAM111B
(F629L +1 more)
Single nucleotide variant
(missense variant)
not provided
GLikely pathogenic
FAM111B
(L609P +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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