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

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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_032737.4(LMNB2):c.574G>T (p.Ala192Ser)	rs112419003	0.00033
NM_032737.4(LMNB2):c.802G>A (p.Asp268Asn)	rs1013986586	0.00003
NM_032737.4(LMNB2):c.1163T>G (p.Ile388Ser)
NM_032737.4(LMNB2):c.1677C>G (p.Ser559Arg)
NM_032737.4(LMNB2):c.859G>A (p.Asp287Asn)
NM_032737.4(LMNB2):c.889_891del (p.Asp297del)

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