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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RPGRIP1L
(N210D)
Single nucleotide variant
(missense variant)
Familial aplasia of the vermis
+7 more
GUncertain significance
RPGRIP1L
(L57F)
Single nucleotide variant
(missense variant)
Meckel syndrome, type 5
+5 more
GConflicting classifications of pathogenicity