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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ABCB7
(R314Q +4 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GBenign/Likely benign
ABCB7, LOC130068449
Single nucleotide variant
(intron variant)
not provided
+1 more
GBenign