List of variants in gene LBR reported as likely benign for autoimmune disease

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_002296.4(LBR):c.843A>G (p.Val281=)	rs61749339	0.01280
NM_002296.4(LBR):c.1315-13T>C	rs201793983	0.00041

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