List of variants in gene combination NEB, RIF1 reported as likely benign 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: 16

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HGVS	dbSNP	gnomAD frequency
NM_001164508.2(NEB):c.25367C>T (p.Thr8456Met)	rs78592085	0.00208
NM_001164508.2(NEB):c.21685G>C (p.Asp7229His)	rs201979610	0.00182
NM_001164508.2(NEB):c.22878C>A (p.Ala7626=)	rs185574478	0.00145
NM_001164508.2(NEB):c.23267T>C (p.Met7756Thr)	rs201767727	0.00108
NM_001164508.2(NEB):c.21419T>C (p.Ile7140Thr)	rs200112795	0.00077
NM_001164508.2(NEB):c.22005G>A (p.Thr7335=)	rs201400523	0.00072
NM_001164508.2(NEB):c.25038A>G (p.Gln8346=)	rs184319249	0.00069
NM_001164508.2(NEB):c.21522T>C (p.Asp7174=)	rs185169373	0.00029
NM_001164508.2(NEB):c.23013C>T (p.Ser7671=)	rs370873040	0.00029
NM_001164508.2(NEB):c.24820T>C (p.Leu8274=)	rs372203426	0.00005
NM_001164508.2(NEB):c.21735T>C (p.Asn7245=)	rs568248647	0.00001
NM_001164508.2(NEB):c.21906C>T (p.Asn7302=)	rs757845188	0.00001
NM_001164508.2(NEB):c.21976A>C (p.Arg7326=)	rs780790042	0.00001
NM_001164508.2(NEB):c.22629C>T (p.Pro7543=)	rs373263895	0.00001
NM_001164508.2(NEB):c.22986T>C (p.His7662=)	rs149606244	0.00001
NM_001164508.2(NEB):c.25236A>G (p.Ser8412=)	rs1574544943

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