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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MAP3K4
(N1003K +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GBenign
MAP3K4
Single nucleotide variant
(intron variant)
not provided
GLikely benign
MAP3K4
Single nucleotide variant
(intron variant)
not provided
GBenign
SERAC1, SLC22A1
+26 more
Deletion
not provided
GPathogenic
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