List of variants in gene combination NEB, RIF1 reported as likely pathogenic by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 13

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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.22590+2T>C	rs200449517	0.00009
NM_001164508.2(NEB):c.24113C>A (p.Ser8038Ter)	rs1458048713	0.00006
NM_001164508.2(NEB):c.21793C>T (p.Arg7265Ter)	rs750900690	0.00001
NM_001164508.2(NEB):c.22170C>G (p.Tyr7390Ter)	rs748922882	0.00001
NM_001164508.2(NEB):c.22489C>T (p.Arg7497Ter)	rs760935667	0.00001
NM_001164508.2(NEB):c.24353_24356dup (p.Met8119fs)	rs1257495033	0.00001
NM_001164508.2(NEB):c.23140C>T (p.Arg7714Ter)	rs1575714905
NM_001164508.2(NEB):c.23628_23631del (p.Gln7876fs)	rs1161478770
NM_001164508.2(NEB):c.24339_24342del (p.Pro8114fs)	rs934111355
NM_001164508.2(NEB):c.24911_24914dup (p.Phe8305fs)	rs2152822941
NM_001164508.2(NEB):c.25214del (p.Gly8405fs)	rs1553520266
NM_001164508.2(NEB):c.25297+1G>A	rs113525641

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