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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130067168, XBP1
(A32V)
Single nucleotide variant
(missense variant)
Autosomal dominant polycystic liver disease
GLikely benign
LOC130067168, XBP1
(P15L)
Single nucleotide variant
(missense variant)
Autosomal dominant polycystic liver disease
GLikely benign
LOC130067168, XBP1
Duplication
(inframe_insertion)
Autosomal dominant polycystic liver disease
GLikely benign
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