List of variants reported as likely benign for Mannose-binding lectin deficiency

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_001378373.1(MBL2):c.378C>G (p.Leu126=)	rs930507	0.77778
NM_001378373.1(MBL2):c.*1691G>A	rs10824792	0.48249
NM_001378373.1(MBL2):c.*2219A>C	rs2083771	0.33140
NM_001378373.1(MBL2):c.*2048A>G	rs2099902	0.33061
NM_001378373.1(MBL2):c.*2388T>G	rs2506	0.32397
NC_000010.11:g.52771701G>A	rs7095891	0.30009
NM_001378373.1(MBL2):c.*1275T>C	rs10082466	0.29126
NM_001378373.1(MBL2):c.*1879A>C	rs2120131	0.28974
NM_001378373.1(MBL2):c.*1913C>T	rs2165813	0.28952
NM_001378373.1(MBL2):c.*1857A>G	rs2120132	0.28354
NM_001378373.1(MBL2):c.*2040G>T	rs2099903	0.28243
NM_001378373.1(MBL2):c.161G>A (p.Gly54Asp)	rs1800450	0.11335
NM_001378373.1(MBL2):c.170G>A (p.Gly57Glu)	rs1800451	0.07628

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