List of variants in gene NOD2 reported as 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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001370466.1(NOD2):c.453C>G (p.Ser151=)	rs2067085	0.35090
NM_001370466.1(NOD2):c.1680T>G (p.Arg560=)	rs1861759	0.32445
NM_001370466.1(NOD2):c.721C>T (p.Pro241Ser)	rs2066842	0.17968
NM_001370466.1(NOD2):c.1296C>T (p.Arg432=)	rs2066843	0.17266
NM_001370466.1(NOD2):c.2782G>A (p.Val928Ile)	rs5743291	0.06122
NM_001370466.1(NOD2):c.2023C>T (p.Arg675Trp)	rs2066844	0.02936
NM_001370466.1(NOD2):c.2381+10A>C	rs72796353	0.01447
NM_001370466.1(NOD2):c.2093C>G (p.Ala698Gly)	rs5743278	0.01319
NM_001370466.1(NOD2):c.2288G>A (p.Arg763Gln)	rs5743279	0.01035
NM_001370466.1(NOD2):c.1372C>T (p.Leu458=)	rs5743274	0.01031
NM_001370466.1(NOD2):c.1752C>T (p.Ala584=)	rs61736932	0.00840
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.735C>T (p.Ser245=)	rs35090774	0.00360
NM_001370466.1(NOD2):c.2325G>T (p.Val775=)	rs104895495	0.00157

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