List of variants in gene NOD2 reported by Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		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.2782G>A (p.Val928Ile)	rs5743291	0.06122
NM_001370466.1(NOD2):c.1752C>T (p.Ala584=)	rs61736932	0.00840
NM_001370466.1(NOD2):c.2042G>A (p.Arg681His)	rs35285618	0.00681
NM_001370466.1(NOD2):c.785A>G (p.Asn262Ser)	rs5743271	0.00557
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.2474A>G (p.Asn825Ser)	rs104895467	0.00076
NM_001370466.1(NOD2):c.2506A>G (p.Met836Val)	rs104895447	0.00073
NM_001370466.1(NOD2):c.2672C>A (p.Ala891Asp)	rs104895452	0.00051
NM_001370466.1(NOD2):c.1036C>T (p.Arg346Cys)	rs145293873	0.00021
NM_001370466.1(NOD2):c.2087C>T (p.Pro696Leu)	rs201076024	0.00011
NM_001370466.1(NOD2):c.1088A>T (p.Asp363Val)	rs769622495	0.00004

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