List of variants in gene combination NEB, RIF1 reported as pathogenic by Natera, Inc.

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_001164508.2(NEB):c.25336C>T (p.Arg8446Ter)	rs200731870	0.00004
NM_001164508.2(NEB):c.22831C>T (p.Arg7611Ter)	rs555582398	0.00001
NM_001164508.2(NEB):c.24395_24398dup (p.Leu8133fs)	rs762133567	0.00001
NM_001164508.2(NEB):c.24527_24528del (p.Pro8176fs)	rs555445835	0.00001
NM_001164508.2(NEB):c.24177_24178del (p.Arg8059fs)	rs1266535163
NM_001164508.2(NEB):c.24209_24212dup (p.Leu8071fs)	rs781667543
NM_001164508.2(NEB):c.24267_24270del (p.Arg8090fs)	rs747564597
NM_001164508.2(NEB):c.24267_24270dup (p.Val8091fs)	rs747564597
NM_001164508.2(NEB):c.24302_24305dup (p.Leu8102fs)	rs1344099907
NM_001164508.2(NEB):c.24549_24550del (p.Arg8183fs)	rs755863625
NM_001164508.2(NEB):c.24579G>C (p.Ser8193=)	rs202048855
NM_001164508.2(NEB):c.24666del (p.Phe8222fs)	rs794727136
NM_001164508.2(NEB):c.24735_24736del (p.Arg8245fs)	rs776059611
NM_001164508.2(NEB):c.25136T>G (p.Leu8379Ter)	rs760200697

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