RS104886142 COL4A5

Health Risk Chr X:108598793
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
X-linked Alport syndrome
Glomerulopathy
Hypertensive disorder
Mild proteinuria
Alport syndrome
COL4A5-related disorder
Monogenic hearing loss
X-linked Alport syndrome
X-linked Alport syndrome
Glomerulopathy
Hypertensive disorder
Mild proteinuria
Alport syndrome
COL4A5-related disorder
Monogenic hearing loss
Other Variants in COL4A5
rs104886229 rs104886121 rs104886091 rs104886043 rs104886303 rs104886308 rs281874765 rs104886050 rs104886427 rs281874760
Ask Dr. Hemsworth about this variant