Variants in gene combination NEB, RIF1 with conflicting interpretations reported as "pathogenic and "uncertain significance"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 6

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HGVS	dbSNP	gnomAD frequency
NM_001164508.2(NEB):c.23989C>T (p.Arg7997Ter)	rs549794342	0.00061
NM_001164508.2(NEB):c.21417+3A>G	rs148950085	0.00004
NM_001164508.2(NEB):c.23910_23913dup (p.Glu7972fs)	rs761694639
NM_001164508.2(NEB):c.23937C>G (p.Tyr7979Ter)	rs779173742
NM_001164508.2(NEB):c.23967_23970del (p.Pro7990fs)	rs756384471
NM_001164508.2(NEB):c.24014_24015dup (p.Ser8006fs)	rs1553568357

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