RS119103273 NCF1

Health Risk Chr 7:74783060 snv missense variant
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What This Variant Does
"[OMIM:?]
Associated Conditions
Granulomatous disease
chronic
autosomal recessive
cytochrome b-positive
type 1
Granulomatous disease
chronic
autosomal recessive
cytochrome b-positive
type 1
Population Frequencies
gnomAD ALL
0%
Other Variants in NCF1
rs4029402 rs1563003964 rs119103270 rs1307080411 rs119103271 rs119103272 rs886041799 rs1057519503 rs145360423 rs782800778
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