List of variants in gene CXCR4 reported as benign for WHIM syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_003467.3(CXCR4):c.414C>T (p.Ile138=)	rs2228014	0.03364
NM_003467.3(CXCR4):c.783C>T (p.Ile261=)	rs148279552	0.00242
NM_003467.3(CXCR4):c.157A>C (p.Ile53Leu)	rs56400844	0.00041
NM_003467.3(CXCR4):c.945C>T (p.His315=)	rs144110709	0.00029
NM_003467.3(CXCR4):c.511G>A (p.Asp171Asn)	rs199535487	0.00015
NM_003467.3(CXCR4):c.250G>C (p.Asp84His)	rs368016542	0.00003
NM_003467.3(CXCR4):c.295G>A (p.Val99Met)	rs755899324	0.00002
NM_003467.3(CXCR4):c.171A>G (p.Gly57=)	rs533290861	0.00001
NM_003467.3(CXCR4):c.529G>A (p.Val177Ile)	rs767830104
NM_003467.3(CXCR4):c.946G>A (p.Ala316Thr)	rs145335491

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