RS1064796094 COL4A3

Health Risk Chr 2:227290086
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What This Variant Does
"CLNSIG=4
Associated Conditions
Autosomal dominant Alport syndrome
Autosomal recessive Alport syndrome
Benign familial hematuria
Autosomal dominant Alport syndrome
Autosomal recessive Alport syndrome
Benign familial hematuria
Other Variants in COL4A3
rs121912824 rs121912825 rs1325453230 rs121912826 rs121912827 rs267606745 rs759739044 rs876657397 rs869025328 rs869025326
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