RS878853089 COL4A5

Health Risk Chr X:108621848
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What This Variant Does
"CLNSIG=4
Associated Conditions
X-linked Alport syndrome
X-linked Alport syndrome
Inborn genetic diseases
X-linked Alport syndrome
X-linked Alport syndrome
Inborn genetic diseases
Other Variants in COL4A5
rs104886229 rs104886121 rs104886091 rs104886043 rs104886303 rs104886308 rs281874765 rs104886050 rs104886427 rs281874760
Ask Dr. Hemsworth about this variant