RS796065030 NCF2

Health Risk Chr 1:183574587
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What This Variant Does
"CLNSIG=5
Associated Conditions
Granulomatous disease
chronic
autosomal recessive
cytochrome b-positive
type 2
Granulomatous disease
chronic
autosomal recessive
cytochrome b-positive
type 2
Other Variants in NCF2
rs374402066 rs796065031 rs796065032 rs119103276 rs796065033 rs119103274 rs137854508 rs755796920 rs147415774 rs367946786
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