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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TMEM67
(A535D +1 more)
Single nucleotide variant
(missense variant +1 more)
COACH syndrome 1
GLikely pathogenic
TMEM67
(R711G +1 more)
Single nucleotide variant
(missense variant +1 more)
Meckel syndrome, type 3
+7 more
GConflicting classifications of pathogenicity