List of variants in gene CXCR1 reported as uncertain significance by Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000634.3(CXCR1):c.3G>A (p.Met1Ile)	rs55808468	0.00516
NM_000634.3(CXCR1):c.838C>T (p.Arg280Cys)	rs61755739	0.00019
NM_000634.3(CXCR1):c.608G>A (p.Arg203Gln)	rs538588993	0.00017

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