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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129929542, SDHB
Single nucleotide variant
(splice donor variant)
Hereditary cancer-predisposing syndrome
+6 more
GPathogenic/Likely pathogenic
LOC129929542, SDHB
(C22S)
Single nucleotide variant
(missense variant)
Paragangliomas 4
+6 more
GConflicting classifications of pathogenicity