RS876657377 NCF4

Health Risk Chr 22:36864944
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Granulomatous disease
chronic
autosomal recessive
cytochrome b-positive
type 3
Granulomatous disease
chronic
autosomal recessive
cytochrome b-positive
type 3
Other Variants in NCF4
rs1940184559 rs766525712 rs567656365 rs112273712 rs1327793505 rs758210984 rs2517929064 rs2548810898 rs2517920041 rs2517929080
Ask Dr. Hemsworth about this variant