List of variants in gene CYP11B1 reported by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000497.4(CYP11B1):c.294G>A (p.Glu98=)	rs143211108	0.00034
NM_000497.4(CYP11B1):c.125C>T (p.Pro42Leu)	rs193922538	0.00008
NM_000497.4(CYP11B1):c.157C>T (p.Leu53=)	rs61751135	0.00005
NM_000497.4(CYP11B1):c.222A>G (p.Glu74=)	rs200096159	0.00003
NM_000497.4(CYP11B1):c.124C>T (p.Pro42Ser)	rs104894069	0.00001
NM_000497.4(CYP11B1):c.270T>C (p.Cys90=)	rs778601992	0.00001
NM_000497.4(CYP11B1):c.281C>T (p.Pro94Leu)	rs104894070
NM_000497.4(CYP11B1):c.385G>A (p.Val129Met)	rs377423817

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