List of variants in gene LBR reported as uncertain significance 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_002296.4(LBR):c.1640A>G (p.Asn547Ser)	rs374343844	0.00004
NM_002296.4(LBR):c.1747C>T (p.Arg583Ter)	rs1057516045	0.00002
NM_002296.4(LBR):c.1757G>A (p.Arg586His)	rs573510559	0.00002
NM_002296.4(LBR):c.1366C>G (p.Leu456Val)	rs377110126	0.00001
NM_002296.4(LBR):c.860T>C (p.Ile287Thr)	rs201093644	0.00001
NM_002296.4(LBR):c.166-12C>T

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