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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SKIC2
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign/Likely benign
SKIC2
(V569M)
Single nucleotide variant
(missense variant)
Trichohepatoenteric syndrome 2
+2 more
GBenign/Likely benign
SKIC2
Single nucleotide variant
(synonymous variant)
Trichohepatoenteric syndrome 2
+1 more
GBenign/Likely benign
SKIC2
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign/Likely benign
SKIC2
(R1063*)
Single nucleotide variant
(nonsense)
Trichohepatoenteric syndrome
+3 more
GPathogenic
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