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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130001468, VLDLR
+1 more
Single nucleotide variant
(non-coding transcript variant +1 more)
VLDLR-related condition
+4 more
GBenign/Likely benign
LOC130001468, VLDLR
+1 more
Single nucleotide variant
(intron variant +1 more)
not specified
+3 more
GBenign