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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CFH
(K224N)
Single nucleotide variant
(missense variant)
Hemolytic uremic syndrome, atypical, susceptibility to, 1
+1 more
GConflicting classifications of pathogenicity
CFH
(Y344C)
Single nucleotide variant
(missense variant)
Factor H deficiency
GUncertain significance
CFH
(I1150R)
Single nucleotide variant
(missense variant)
Hemolytic uremic syndrome, atypical, susceptibility to, 1
GUncertain significance
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