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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SDHA
(R31*)
Single nucleotide variant
(nonsense)
Leigh syndrome
+9 more
GPathogenic/Likely pathogenic
SDHA
(F160L +1 more)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1GG
+3 more
GConflicting classifications of pathogenicity
SDHA
(E182fs +1 more)
Deletion
(frameshift variant)
not provided
+5 more
GPathogenic/Likely pathogenic
SDHA
(R451S +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+3 more
GConflicting classifications of pathogenicity
SDHA
Single nucleotide variant
(splice acceptor variant)
Hereditary cancer-predisposing syndrome
+2 more
GPathogenic/Likely pathogenic
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