RS778034451 COL4A3

Health Risk Chr 2:227273117
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What This Variant Does
"CLNSIG=4
Associated Conditions
Alport syndrome
Autosomal recessive Alport syndrome
Autosomal dominant Alport syndrome
Hematuria
benign familial
2
Alport syndrome 3b
autosomal recessive
Alport syndrome
Autosomal recessive Alport syndrome
Autosomal dominant Alport syndrome
Hematuria
benign familial
2
Alport syndrome 3b
Other Variants in COL4A3
rs121912824 rs121912825 rs1325453230 rs121912826 rs121912827 rs267606745 rs759739044 rs876657397 rs869025328 rs869025326
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