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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RIPK1
(T645M +2 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
ACADSB
(P249fs +1 more)
Deletion
(frameshift variant)
See cases
+1 more
GLikely pathogenic
PYGM
(R650* +1 more)
Single nucleotide variant
(nonsense)
Glycogen storage disease, type V
GPathogenic
SLCO1B1
Single nucleotide variant
(splice donor variant)
See cases
GLikely risk allele
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