List of variants in gene NOD2 reported as likely benign for Autoinflammatory syndrome

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: 43

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HGVS	dbSNP	gnomAD frequency
NM_001370466.1(NOD2):c.2717+158C>T	rs5743289	0.10180
NM_001370466.1(NOD2):c.460-3T>C	rs141833420	0.00836
NM_001370466.1(NOD2):c.337G>A (p.Ala113Thr)	rs34684955	0.00726
NM_001370466.1(NOD2):c.974A>G (p.His325Arg)	rs5743272	0.00389
NM_001370466.1(NOD2):c.2183C>T (p.Ala728Val)	rs61747625	0.00307
NM_001370466.1(NOD2):c.485C>T (p.Thr162Met)	rs61755182	0.00291
NM_001370466.1(NOD2):c.1188G>T (p.Val396=)	rs77966199	0.00273
NM_001370466.1(NOD2):c.2325G>T (p.Val775=)	rs104895495	0.00157
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.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.293C>T (p.Pro98Leu)	rs149390911	0.00076
NM_001370466.1(NOD2):c.2506A>G (p.Met836Val)	rs104895447	0.00073
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.486G>A (p.Thr162=)	rs144887729	0.00051
NM_001370466.1(NOD2):c.193G>A (p.Val65Ile)	rs187264529	0.00048
NM_001370466.1(NOD2):c.1464G>T (p.Leu488=)	rs553575063	0.00042
NM_001370466.1(NOD2):c.1969C>T (p.Arg657Trp)	rs5743276	0.00032
NM_001370466.1(NOD2):c.662T>G (p.Leu221Arg)	rs104895423	0.00026
NM_001370466.1(NOD2):c.1922C>T (p.Pro641Leu)	rs5743275	0.00024
NM_001370466.1(NOD2):c.1036C>T (p.Arg346Cys)	rs145293873	0.00021
NM_001370466.1(NOD2):c.1923G>A (p.Pro641=)	rs199475914	0.00019
NM_001370466.1(NOD2):c.2066G>A (p.Arg689His)	rs200035357	0.00018
NM_001370466.1(NOD2):c.1275C>T (p.Ile425=)	rs186719861	0.00014
NM_001370466.1(NOD2):c.2389G>A (p.Asp797Asn)	rs61755272	0.00014
NM_001370466.1(NOD2):c.402C>T (p.Phe134=)	rs565504727	0.00008
NM_001370466.1(NOD2):c.1875G>A (p.Ser625=)	rs141355588	0.00007
NM_001370466.1(NOD2):c.403G>A (p.Val135Ile)	rs139571975	0.00005
NM_001370466.1(NOD2):c.1088A>T (p.Asp363Val)	rs769622495	0.00004
NM_001370466.1(NOD2):c.1322G>A (p.Arg441His)	rs775728252	0.00004
NM_001370466.1(NOD2):c.2024G>A (p.Arg675Gln)	rs139104022	0.00004
NM_001370466.1(NOD2):c.2465C>T (p.Ala822Val)	rs104895486	0.00003
NM_001370466.1(NOD2):c.2572G>C (p.Ala858Pro)	rs759456303	0.00003
NM_001370466.1(NOD2):c.1091G>A (p.Arg364His)	rs554887705	0.00001
NM_001370466.1(NOD2):c.359G>A (p.Ser120Asn)	rs776403451	0.00001
NM_001370466.1(NOD2):c.545C>T (p.Pro182Leu)	rs753744335	0.00001
NM_001370466.1(NOD2):c.255C>T (p.Ala85=)	rs770046355

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