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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130055850, MAX
(V9L)
Single nucleotide variant
(missense variant +1 more)
not specified
+4 more
GUncertain significance
LOC130055850, MAX
Microsatellite
(5 prime UTR variant)
not provided
+1 more
GConflicting classifications of pathogenicity