RS569681869 COL4A4

Health Risk Chr 2:227059468
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What This Variant Does
"CLNSIG=5
Associated Conditions
Myopia
Hypertensive disorder
Hematuria
Proteinuria
Hearing impairment
Autosomal recessive Alport syndrome
Alport syndrome
Benign familial hematuria
benign familial
1
Myopia
Hypertensive disorder
Hematuria
Proteinuria
Hearing impairment
Other Variants in COL4A4
rs121912858 rs121912859 rs121912860 rs121912861 rs121912862 rs121912863 rs1559493506 rs769783985 rs267599231 rs786205548
Ask Dr. Hemsworth about this variant