RS771943519 COL4A4

Health Risk Chr 2:227144544
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What This Variant Does
"CLNSIG=4
Associated Conditions
Autosomal dominant Alport syndrome
Alport syndrome
Hematuria
Benign familial hematuria
Autosomal recessive Alport syndrome
Microscopic hematuria
Inborn genetic diseases
Autosomal dominant Alport syndrome
Alport syndrome
Hematuria
Benign familial hematuria
Autosomal recessive Alport syndrome
Microscopic hematuria
Inborn genetic diseases
Other Variants in COL4A4
rs121912858 rs121912859 rs121912860 rs121912861 rs121912862 rs121912863 rs1559493506 rs769783985 rs267599231 rs786205548
Ask Dr. Hemsworth about this variant