RS267606745 COL4A3

Health Risk Chr 2:227295044
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal dominant Alport syndrome
Autosomal recessive Alport syndrome
Alport syndrome
Alport syndrome 3b
autosomal recessive
Hematuria
benign familial
2
Autosomal dominant Alport syndrome
Autosomal recessive Alport syndrome
Alport syndrome
Alport syndrome 3b
autosomal recessive
Hematuria
benign familial
Other Variants in COL4A3
rs121912824 rs121912825 rs1325453230 rs121912826 rs121912827 rs759739044 rs876657397 rs869025328 rs869025326 rs869025327
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