List of variants in gene LMNB2 reported as pathogenic for autosomal dominant primary microcephaly

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_032737.4(LMNB2):c.1192G>A (p.Glu398Lys)	rs1971791380
NM_032737.4(LMNB2):c.160A>C (p.Asn54His)	rs1972096108
NM_032737.4(LMNB2):c.578_579del (p.Val193fs)

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