List of variants in gene CYP4F22 reported as uncertain significance by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_173483.4(CYP4F22):c.463C>T (p.His155Tyr)	rs141382984	0.00140
NM_173483.4(CYP4F22):c.874G>A (p.Glu292Lys)	rs139163760	0.00021
NM_173483.4(CYP4F22):c.850C>T (p.Arg284Trp)	rs199782025	0.00007
NM_173483.4(CYP4F22):c.314C>T (p.Pro105Leu)	rs749972738	0.00002
NM_173483.4(CYP4F22):c.1475C>T (p.Thr492Ile)	rs2513164035
NM_173483.4(CYP4F22):c.169C>T (p.Arg57Cys)
NM_173483.4(CYP4F22):c.376_377delinsAA (p.Ala126Asn)
NM_173483.4(CYP4F22):c.839A>T (p.Gln280Leu)
NM_173483.4(CYP4F22):c.999G>T (p.Met333Ile)	rs1555729701

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