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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SDHC
(K86E +2 more)
Single nucleotide variant
(missense variant +2 more)
SDHC-related condition
+6 more
GConflicting classifications of pathogenicity
SDHC
(E144Q +2 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+6 more
GConflicting classifications of pathogenicity
SDHC
Single nucleotide variant
(3 prime UTR variant)
not provided
+2 more
GBenign
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