RS149938052 CFH

Health Risk Chr 1:196740780
Upload your DNA to see your genotype for this variant.
Associated Conditions
CFH-Related Dense Deposit Disease / Membranoproliferative Glomerulonephritis Type II
Age related macular degeneration 4
Basal laminar drusen
Hemolytic uremic syndrome
atypical
susceptibility to
1
Factor H deficiency
Inborn genetic diseases
Atypical hemolytic-uremic syndrome
CFH-Related Dense Deposit Disease / Membranoproliferative Glomerulonephritis Type II
Age related macular degeneration 4
Basal laminar drusen
Hemolytic uremic syndrome
atypical
Other Variants in CFH
rs121913051 rs460897 rs796052136 rs121913054 rs1061170 rs121913056 rs796052137 rs121913057 rs121913058 rs796052138
Ask Dr. Hemsworth about this variant