List of variants reported as likely benign for Blau syndrome; Inflammatory bowel disease 1

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_001370466.1(NOD2):c.2717+158C>T	rs5743289	0.10180
NM_001370466.1(NOD2):c.-8-2185C>T	rs144993105	0.00024
NM_001370466.1(NOD2):c.1923G>A (p.Pro641=)	rs199475914	0.00019
NM_001370466.1(NOD2):c.510C>T (p.Ala170=)	rs765729513	0.00002
NM_001370466.1(NOD2):c.1755G>A (p.Ala585=)	rs756626309	0.00001
NM_001370466.1(NOD2):c.2022C>T (p.Leu674=)	rs1459264285
NM_001370466.1(NOD2):c.216C>T (p.Ala72=)	rs1398956455
NM_001370466.1(NOD2):c.2586A>C (p.Gln862His)	rs764244331
NM_001370466.1(NOD2):c.2652G>A (p.Val884=)	rs1359941511
NM_001370466.1(NOD2):c.2881C>T (p.Leu961=)	rs1596908135
NM_001370466.1(NOD2):c.9G>A (p.Ser3=)	rs774491311

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