List of variants in gene LBR studied for Pelger-Huët anomaly; Greenberg dysplasia; Reynolds syndrome; Regressive spondylometaphyseal dysplasia

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 5

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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
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

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