RS869025328 COL4A3
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What This Variant Does
"CLNSIG=5
Associated Conditions
Benign familial hematuria
Autosomal dominant Alport syndrome
Hematuria
benign familial
2
Alport syndrome 3b
autosomal recessive
Autosomal recessive Alport syndrome
Autosomal dominant Alport syndrome
Benign familial hematuria
Alport syndrome 3b
autosomal recessive
Alport syndrome
Hematuria
benign familial
Other Variants in COL4A3