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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KRT18, KRT8
+1 more
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
KRT18, LOC106096416
(S230T)
Single nucleotide variant
(missense variant)
not provided
GLikely benign