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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CFHR4
(Y34H +1 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GLikely benign
CFHR4
(R39C +1 more)
Single nucleotide variant
(missense variant)
Kidney disorder
GUncertain significance
CFHR4
(Y42F +1 more)
Single nucleotide variant
(missense variant)
Atypical hemolytic-uremic syndrome
GLikely benign
CFHR4
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign/Likely benign
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