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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129936665, SETD2
(P23R)
Single nucleotide variant
(5 prime UTR variant +2 more)
Luscan-Lumish syndrome
GUncertain significance
LOC129936665, SETD2
(Q7*)
Single nucleotide variant
(5 prime UTR variant +2 more)
not specified
+3 more
GConflicting classifications of pathogenicity