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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MCM8
(I138M)
Single nucleotide variant
(missense variant)
not provided
+1 more
GBenign
MCM8
(R278C)
Single nucleotide variant
(missense variant)
MCM8-related condition
GLikely benign
MCM8
Single nucleotide variant
(synonymous variant)
MCM8-related condition
GBenign
MCM8
(R640Q +3 more)
Single nucleotide variant
(missense variant)
MCM8-related condition
GBenign
MCM8, MCM8-AS1
(S717F +3 more)
Single nucleotide variant
(missense variant)
MCM8-related condition
GLikely benign
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