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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
C3
(I1367T)
Single nucleotide variant
(missense variant)
not specified
+1 more
GConflicting classifications of pathogenicity
C3
(G1224D)
Single nucleotide variant
(missense variant)
Atypical hemolytic-uremic syndrome with C3 anomaly
+4 more
GConflicting classifications of pathogenicity
C3
(Q1198R)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
C3
(K633R)
Single nucleotide variant
(missense variant)
Age related macular degeneration 9
+3 more
GConflicting classifications of pathogenicity
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