RS104886312 COL4A5

Health Risk Chr X:108591645
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal dominant Alport syndrome
Thyroid cancer
nonmedullary
1
Autosomal dominant Alport syndrome
Thyroid cancer
nonmedullary
1
Other Variants in COL4A5
rs104886229 rs104886121 rs104886091 rs104886043 rs104886303 rs104886308 rs281874765 rs104886050 rs104886427 rs281874760
Ask Dr. Hemsworth about this variant