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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CFH, CFHR1
+1 more
Deletion
Hemolytic uremic syndrome, atypical, susceptibility to, 1
GPathogenic
CFH
(S1191L)
Single nucleotide variant
(missense variant)
CFH-Related Disorders
+5 more
GPathogenic
CFH
(V1197A)
Single nucleotide variant
(missense variant)
not provided
+4 more
GPathogenic/Likely pathogenic
CFH
(R1210C)
Single nucleotide variant
(missense variant)
Kidney disorder
+6 more
GConflicting classifications of pathogenicity
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