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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHRNE
(S467G)
Single nucleotide variant
(missense variant)
See cases
GUncertain significance
C17orf107, CHRNE
(P302R)
Single nucleotide variant
(3 prime UTR variant +1 more)
See cases
+3 more
GConflicting classifications of pathogenicity