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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ASIC4-AS1, SPEG
(R2747C)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ASIC4-AS1, GMPPA
(F198L)
Single nucleotide variant
(missense variant)
Alacrima, achalasia, and intellectual disability syndrome
+1 more
GConflicting classifications of pathogenicity