RS121912824 COL4A3

Health Risk Chr 2:227307898
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What This Variant Does
"[OMIM:?]
Associated Conditions
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
2
Other Variants in COL4A3
rs121912825 rs1325453230 rs121912826 rs121912827 rs267606745 rs759739044 rs876657397 rs869025328 rs869025326 rs869025327
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