List of variants in gene NEB reported as likely pathogenic by CeGaT Center for Human Genetics Tuebingen

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_001164508.2(NEB):c.18024_18027del (p.Val6009fs)	rs748358450
NM_001164508.2(NEB):c.3858C>A (p.Cys1286Ter)	rs1386238241
NM_001164508.2(NEB):c.4507-2A>G	rs1575668113

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