List of variants in gene CXCR2 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001557.4(CXCR2):c.458G>A (p.Arg153His)	rs55799208	0.00139
NM_001557.4(CXCR2):c.1075A>T (p.Thr359Ser)	rs150629039	0.00007
NM_001557.4(CXCR2):c.707G>A (p.Arg236His)	rs144013681	0.00002
NM_001557.4(CXCR2):c.476G>T (p.Arg159Leu)	rs368809767
NM_001557.4(CXCR2):c.488A>T (p.Lys163Ile)	rs1574542767

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