List of variants in gene combination NEB, RIF1 reported as benign by GeneDx

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: 26

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HGVS	dbSNP	gnomAD frequency
NM_001164508.2(NEB):c.24766-18C>T	rs2288195	0.64910
NM_001164508.2(NEB):c.24433G>C (p.Ala8145Pro)	rs7575451	0.64120
NM_001164508.2(NEB):c.21585A>G (p.Thr7195=)	rs4664475	0.55659
NM_001164508.2(NEB):c.25204A>G (p.Ile8402Val)	rs1061305	0.40617
NM_001164508.2(NEB):c.25150+12G>A	rs4414676	0.07283
NM_001164508.2(NEB):c.25395T>G (p.Ser8465=)	rs13031275	0.03886
NM_001164508.2(NEB):c.21963A>G (p.Lys7321=)	rs61730765	0.03096
NM_001164508.2(NEB):c.21382T>C (p.Leu7128=)	rs114218081	0.02752
NM_001164508.2(NEB):c.23381C>T (p.Ser7794Leu)	rs41270201	0.01730
NM_001164508.2(NEB):c.21856G>A (p.Asp7286Asn)	rs35625617	0.01691
NM_001164508.2(NEB):c.23511G>A (p.Thr7837=)	rs35808744	0.01201
NM_001164508.2(NEB):c.23495C>T (p.Thr7832Ile)	rs34368668	0.01129
NM_001164508.2(NEB):c.21519C>T (p.Ser7173=)	rs16830170	0.00961
NM_001164508.2(NEB):c.24208-7C>T	rs113048349	0.00793
NM_001164508.2(NEB):c.24264G>A (p.Met8088Ile)	rs144709880	0.00436
NM_001164508.2(NEB):c.22904G>A (p.Gly7635Glu)	rs3732309	0.00351
NM_001164508.2(NEB):c.25542C>T (p.Thr8514=)	rs3821324	0.00183
NM_001164508.2(NEB):c.23599A>C (p.Lys7867Gln)	rs118191309	0.00171
NM_001164508.2(NEB):c.21720C>T (p.Tyr7240=)	rs34718443	0.00165
NM_001164508.2(NEB):c.25035C>T (p.Asp8345=)	rs201825451	0.00123
NM_001164508.2(NEB):c.23267T>C (p.Met7756Thr)	rs201767727	0.00108
NM_001164508.2(NEB):c.23055G>A (p.Gly7685=)	rs563896790	0.00010
NM_001164508.2(NEB):c.21418-6del	rs56026241
NM_001164508.2(NEB):c.21546C>T (p.Asn7182=)	rs149510427
NM_001164508.2(NEB):c.22161+18G>C	rs6721666
NM_001164508.2(NEB):c.25405-17dup	rs148839798

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