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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130057714, TMED3
(V5A)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
LOC130057714, TMED3
(P6L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance