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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COL4A2
(G1203D)
Single nucleotide variant
(missense variant)
Hemorrhage, intracerebral, susceptibility to
GUncertain significance
COL4A2-AS1, COL4A2
(G1383R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GPathogenic/Likely pathogenic