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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KRT8, KRT18
+1 more
(R90C)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GBenign/Likely benign
KRT18, KRT8
+1 more
(A92P)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GBenign/Likely benign
KRT18, KRT8
+1 more
(S100R)
Single nucleotide variant
(non-coding transcript variant +2 more)
not provided
+1 more
GBenign/Likely benign
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