RS104886189 COL4A5

Health Risk Chr X:108620354
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What This Variant Does
"[OMIM:?]
Associated Conditions
X-linked Alport syndrome
Atypical hemolytic-uremic syndrome
Alport syndrome
Autosomal dominant Alport syndrome
X-linked Alport syndrome
Atypical hemolytic-uremic syndrome
Alport syndrome
Autosomal dominant Alport syndrome
Other Variants in COL4A5
rs104886229 rs104886121 rs104886091 rs104886043 rs104886303 rs104886308 rs281874765 rs104886050 rs104886427 rs281874760
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