List of variants in gene NOD2 reported as likely benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 34

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HGVS	dbSNP	gnomAD frequency
NM_001370466.1(NOD2):c.785A>G (p.Asn262Ser)	rs5743271	0.00557
NM_001370466.1(NOD2):c.974A>G (p.His325Arg)	rs5743272	0.00389
NM_001370466.1(NOD2):c.2026C>T (p.Arg676Cys)	rs5743277	0.00340
NM_001370466.1(NOD2):c.485C>T (p.Thr162Met)	rs61755182	0.00291
NM_001370466.1(NOD2):c.2291G>A (p.Arg764Gln)	rs104895464	0.00137
NM_001370466.1(NOD2):c.1970G>A (p.Arg657Gln)	rs114664276	0.00131
NM_001370466.1(NOD2):c.2296G>A (p.Val766Met)	rs104895444	0.00127
NM_001370466.1(NOD2):c.1211C>T (p.Ser404Leu)	rs104895431	0.00103
NM_001370466.1(NOD2):c.-8-7T>A	rs104895421	0.00092
NM_001370466.1(NOD2):c.552C>T (p.Ala184=)	rs5743269	0.00090
NM_001370466.1(NOD2):c.1707G>A (p.Thr569=)	rs104895437	0.00086
NM_001370466.1(NOD2):c.2474A>G (p.Asn825Ser)	rs104895467	0.00076
NM_001370466.1(NOD2):c.379G>A (p.Asp127Asn)	rs146054564	0.00068
NM_001370466.1(NOD2):c.1330C>T (p.Arg444Cys)	rs1078327	0.00057
NM_001370466.1(NOD2):c.2057G>A (p.Arg686His)	rs104895483	0.00055
NM_001370466.1(NOD2):c.2672C>A (p.Ala891Asp)	rs104895452	0.00051
NM_001370466.1(NOD2):c.1693G>A (p.Val565Met)	rs148683734	0.00041
NM_001370466.1(NOD2):c.258C>T (p.Asp86=)	rs138889062	0.00041
NM_001370466.1(NOD2):c.2490C>T (p.Asp830=)	rs144083291	0.00039
NM_001370466.1(NOD2):c.760C>T (p.Leu254Phe)	rs756943416	0.00027
NM_001370466.1(NOD2):c.-8-2185C>T	rs144993105	0.00024
NM_001370466.1(NOD2):c.989A>C (p.Asp330Ala)	rs104895469	0.00024
NM_001370466.1(NOD2):c.1522C>T (p.Leu508=)	rs145190613	0.00016
NM_001370466.1(NOD2):c.2382-9T>A	rs201759367	0.00011
NM_001370466.1(NOD2):c.45C>T (p.Val15=)	rs766815592	0.00011
NM_001370466.1(NOD2):c.1608C>T (p.Tyr536=)	rs111608429	0.00010
NM_001370466.1(NOD2):c.2658C>T (p.Asp886=)	rs104895451	0.00003
NM_001370466.1(NOD2):c.1428G>A (p.Glu476=)	rs104895434	0.00001
NM_001370466.1(NOD2):c.1563G>A (p.Leu521=)	rs369085294	0.00001
NM_001370466.1(NOD2):c.2304G>C (p.Leu768=)	rs1164125645	0.00001
NM_001370466.1(NOD2):c.1434G>A (p.Gly478=)	rs769034739
NM_001370466.1(NOD2):c.2550-16_2550-15del	rs762600414
NM_001370466.1(NOD2):c.2641G>C (p.Gly881Arg)	rs2066845
NM_001370466.1(NOD2):c.309A>G (p.Pro103=)	rs2150782456

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