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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TMEM94
(V1193F +4 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GLikely benign
TMEM94
(P1196S +4 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GLikely benign