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Links from MedGen

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MIR9718, SIX1
(R178T)
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
GUncertain significance
COL4A5
(G728R)
Single nucleotide variant
(missense variant)
Mild proteinuria
+2 more
GUncertain significance