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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KMT2B, LOC130064257
(G22S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KMT2B, LOC130064257
Microsatellite
(inframe_insertion +1 more)
not provided
GUncertain significance