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Items: 8

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SEC63
(P536fs)
Duplication
(frameshift variant)
Polycystic liver disease 2
+1 more
GPathogenic/Likely pathogenic
SEC63
Single nucleotide variant
(synonymous variant)
Polycystic liver disease 2
+2 more
GBenign
SEC63
Indel
(intron variant)
Polycystic liver disease 2
+1 more
GBenign/Likely benign
SEC63
Indel
(intron variant)
not specified
GBenign/Likely benign
SEC63
Deletion
(intron variant)
Polycystic liver disease 2
+3 more
GBenign/Likely benign
SEC63
Deletion
(intron variant)
not specified
+2 more
GBenign
SEC63
Single nucleotide variant
(intron variant)
not specified
+1 more
GBenign/Likely benign
SEC63
(R37fs)
Deletion
(frameshift variant)
not provided
GPathogenic
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