List of variants in gene combination CYLD, NOD2 reported as likely benign for immune system disorder

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_001370466.1(NOD2):c.*620G>A	rs116213743	0.00230
NM_001370466.1(NOD2):c.*990T>C	rs192842874	0.00208
NM_001370466.1(NOD2):c.3013G>A (p.Gly1005Ser)	rs147874812	0.00046
NM_001370466.1(NOD2):c.*877C>A	rs140643942	0.00031
NM_001370466.1(NOD2):c.*1023C>T	rs5743299	0.00019
NM_001370466.1(NOD2):c.2979G>A (p.Gly993=)	rs374689495	0.00009
NM_001370466.1(NOD2):c.2886-9C>A	rs554292255	0.00006
NM_001370466.1(NOD2):c.2970-16A>G	rs530365159	0.00002
NM_001370466.1(NOD2):c.3012C>T (p.Leu1004=)	rs201214915	0.00002
NM_001370466.1(NOD2):c.2931G>A (p.Leu977=)	rs773388366	0.00001
NM_001370466.1(NOD2):c.2886-12C>T
NM_001370466.1(NOD2):c.2886-17T>C	rs757094587
NM_001370466.1(NOD2):c.2959C>T (p.Leu987=)
NM_001370466.1(NOD2):c.2969+13G>A
NM_001370466.1(NOD2):c.2969+14G>A	rs2150843410
NM_001370466.1(NOD2):c.2969+15C>A
NM_001370466.1(NOD2):c.2985T>C (p.Thr995=)
NM_022162.3(NOD2):c.3019dup (p.Leu1007fs)	rs2066847

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