RS876657397 COL4A3

Health Risk Chr 2:227164756
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive Alport syndrome
Alport syndrome
COL4A3-related disorder
Inborn genetic diseases
Autosomal dominant Alport syndrome
Alport syndrome 3b
autosomal recessive
Hematuria
benign familial
2
Autosomal recessive Alport syndrome
Alport syndrome
COL4A3-related disorder
Inborn genetic diseases
Autosomal dominant Alport syndrome
Other Variants in COL4A3
rs121912824 rs121912825 rs1325453230 rs121912826 rs121912827 rs267606745 rs759739044 rs869025328 rs869025326 rs869025327
Ask Dr. Hemsworth about this variant