List of variants in gene combination LMNB2, MIR7108 reported as likely benign for childhood-onset epilepsy syndrome

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_032737.4(LMNB2):c.855+8C>T	rs375918278	0.00025
NM_032737.4(LMNB2):c.856-10C>T	rs751305991	0.00001
NM_032737.4(LMNB2):c.856-17C>T	rs777712102	0.00001
NM_032737.4(LMNB2):c.855+14G>A	rs1971803815
NM_032737.4(LMNB2):c.855+16G>A	rs368113823
NM_032737.4(LMNB2):c.855+9G>T	rs772053278
NM_032737.4(LMNB2):c.856-12G>A
NM_032737.4(LMNB2):c.856-8C>T	rs766316644

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