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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CFHR3
(G18A)
Single nucleotide variant
(missense variant)
Atypical hemolytic-uremic syndrome
+1 more
GBenign
CFHR3
(F34C)
Single nucleotide variant
(missense variant)
Hemolytic uremic syndrome, atypical, susceptibility to, 1
+3 more
GBenign/Likely benign
CFHR3
(G119R)
Single nucleotide variant
(missense variant)
Kidney disorder
GUncertain significance
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