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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129999736, MNX1
Microsatellite
(inframe_deletion)
not provided
GLikely benign
LOC129999736, MNX1
(A134del)
Microsatellite
(inframe_deletion)
not provided
GBenign/Likely benign