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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SDHB
(I220T)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+4 more
GUncertain significance
SDHB
(W200C)
Single nucleotide variant
(missense variant)
Gastrointestinal stromal tumor
+5 more
GPathogenic/Likely pathogenic
SDHB
(V140F)
Single nucleotide variant
(missense variant)
not provided
+5 more
GPathogenic/Likely pathogenic
SDHB
(I127S)
Single nucleotide variant
(missense variant)
Hereditary pheochromocytoma-paraganglioma
+5 more
GPathogenic/Likely pathogenic
SDHB
(G53E)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+7 more
GBenign/Likely benign
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