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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
APOB, LOC106560211
Microsatellite
(inframe_insertion)
APOB-related disorder
+4 more
GBenign/Likely benign
APOB, LOC106560211
Microsatellite
(inframe_deletion)
Hypercholesterolemia, familial, 1
+6 more
GBenign/Likely benign