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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TMEM67
Deletion
(intron variant)
not provided
+1 more
GUncertain significance
TMEM67
(E174Q +1 more)
Single nucleotide variant
(missense variant +1 more)
Nephronophthisis 11
GUncertain significance