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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126861339, SDHD
(G16C)
Single nucleotide variant
(missense variant +1 more)
Pheochromocytoma
+5 more
GUncertain significance
SDHD
(H30Y)
Single nucleotide variant
(missense variant +2 more)
Pheochromocytoma
+5 more
GUncertain significance
SDHD
(P81L +1 more)
Single nucleotide variant
(missense variant +2 more)
Pheochromocytoma
+9 more
GPathogenic/Likely pathogenic
SDHD
(D92Y +1 more)
Single nucleotide variant
(missense variant +2 more)
not provided
+6 more
GPathogenic/Likely pathogenic
SDHD
(Y93C +1 more)
Single nucleotide variant
(missense variant +2 more)
Pheochromocytoma
+8 more
GConflicting classifications of pathogenicity
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