List of variants in gene CYP2U1 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_183075.3(CYP2U1):c.671T>C (p.Ile224Thr)	rs139692261	0.00007
NM_183075.3(CYP2U1):c.358T>C (p.Phe120Leu)	rs763896315	0.00005
NM_183075.3(CYP2U1):c.557G>A (p.Arg186His)	rs746319505	0.00001
NM_183075.3(CYP2U1):c.565G>C (p.Gly189Arg)	rs1401706343	0.00001
NM_183075.3(CYP2U1):c.1448T>C (p.Phe483Ser)
NM_183075.3(CYP2U1):c.1472T>G (p.Met491Arg)
NM_183075.3(CYP2U1):c.811A>G (p.Asn271Asp)	rs1057524672

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