List of variants in gene CD19 reported as benign for hematologic disorder

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001770.6(CD19):c.520C>G (p.Leu174Val)	rs2904880	0.76211
NM_001770.6(CD19):c.1541G>A (p.Arg514His)	rs34763945	0.04099
NM_001770.6(CD19):c.1486+18T>A	rs150575329	0.01255
NM_001770.6(CD19):c.705G>T (p.Pro235=)	rs35979293

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