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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOXHD1
Single nucleotide variant
(intron variant)
not specified
+2 more
GBenign/Likely benign
LOXHD1
(G1509E +2 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
LOXHD1
(R1155G +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+2 more
GBenign
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