List of variants in gene CD19 reported as likely benign for immune system 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001770.6(CD19):c.381G>A (p.Ser127=)	rs142342927	0.00523
NM_001770.6(CD19):c.1311C>T (p.Ser437=)	rs148047850	0.00301
NM_001770.6(CD19):c.406C>T (p.Leu136=)	rs117769220	0.00048
NM_001770.6(CD19):c.390T>A (p.Gly130=)	rs573154781	0.00014
NM_001770.6(CD19):c.47T>C (p.Met16Thr)	rs745681190	0.00001

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