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Links from OMIM

Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
VPS33B
(C576R +2 more)
Single nucleotide variant
(missense variant)
Arthrogryposis, renal dysfunction, and cholestasis 1
+1 more
GPathogenic
VPS33B
Single nucleotide variant
(intron variant)
Arthrogryposis, renal dysfunction, and cholestasis 1
+2 more
GPathogenic/Likely pathogenic
VPS33B
(L30P)
Single nucleotide variant
(missense variant +1 more)
Arthrogryposis, renal dysfunction, and cholestasis 1
GPathogenic
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