List of variants in gene LBR reported as uncertain significance for autoimmune disease

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_002296.4(LBR):c.271C>T (p.Pro91Ser)	rs201003932	0.00012
NM_002296.4(LBR):c.505C>T (p.Arg169Cys)	rs2230420	0.00009
NM_002296.4(LBR):c.1640A>G (p.Asn547Ser)	rs374343844	0.00004
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.1097A>G (p.Tyr366Cys)
NM_002296.4(LBR):c.1486T>G (p.Cys496Gly)

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