RS375040636 COL4A3
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What This Variant Does
"CLNSIG=4
Associated Conditions
Autosomal recessive Alport syndrome
Benign familial hematuria
Autosomal dominant Alport syndrome
Autosomal recessive Alport syndrome
Benign familial hematuria
Autosomal dominant Alport syndrome
Other Variants in COL4A3