List of variants in gene combination CYLD, NOD2 reported as 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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001370466.1(NOD2):c.*397A>C	rs3135499	0.45667
NM_001370466.1(NOD2):c.*1156G>A	rs3135500	0.44678
NM_001370466.1(NOD2):c.*521C>T	rs5743297	0.01203
NM_001370466.1(NOD2):c.*873C>T	rs373812846	0.00255
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.*89C>T	rs184545855	0.00183
NM_001370466.1(NOD2):c.2886-16G>C	rs199525467	0.00118
NM_001370466.1(NOD2):c.3013G>A (p.Gly1005Ser)	rs147874812	0.00046
NM_001370466.1(NOD2):c.2886-11T>G	rs200519856	0.00035
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.*8G>A	rs199475923	0.00003
NM_001370466.1(NOD2):c.3015C>A (p.Gly1005=)	rs765204397	0.00002
NM_001370466.1(NOD2):c.*183C>T	rs547264433

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