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Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SDHC
(R15*)
Single nucleotide variant
(nonsense +3 more)
Hereditary cancer-predisposing syndrome
+4 more
GPathogenic
SDHC
(T33M +1 more)
Single nucleotide variant
(missense variant +3 more)
Hereditary cancer-predisposing syndrome
+6 more
GUncertain significance
SDHC
Single nucleotide variant
(synonymous variant +2 more)
Hereditary cancer-predisposing syndrome
+5 more
GBenign/Likely benign
SDHC
(R50C +2 more)
Single nucleotide variant
(missense variant +2 more)
Paragangliomas 3
+4 more
GConflicting classifications of pathogenicity
SDHC
(Y99H +7 more)
Single nucleotide variant
(missense variant +2 more)
Hereditary pheochromocytoma-paraganglioma
+4 more
GConflicting classifications of pathogenicity
SDHC
Single nucleotide variant
(synonymous variant +2 more)
not specified
+5 more
GBenign/Likely benign
SDHC
(Y126C +7 more)
Single nucleotide variant
(missense variant +2 more)
Paragangliomas 3
+5 more
GPathogenic/Likely pathogenic
SDHD
Single nucleotide variant
(synonymous variant +2 more)
Pheochromocytoma
+9 more
GBenign/Likely benign
SDHD
Single nucleotide variant
(synonymous variant +2 more)
Pheochromocytoma
+9 more
GBenign/Likely benign
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