List of variants reported as likely benign for immune system disorder by Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_000250.2(MPO):c.995C>T (p.Ala332Val)	rs28730837	0.01176
NM_000543.5(SMPD1):c.1071C>T (p.Ala357=)	rs72896268	0.00571
NM_000543.5(SMPD1):c.813T>C (p.Pro271=)	rs61876771	0.00500
NM_000543.5(SMPD1):c.901G>A (p.Val301Ile)	rs2723669	0.00374
NM_002273.4(KRT8):c.187A>G (p.Ile63Val)	rs59536457	0.00302
NM_000543.5(SMPD1):c.1091+9C>T	rs143612450	0.00103
NM_000543.5(SMPD1):c.297C>G (p.Thr99=)	rs146630228	0.00072
NM_000543.5(SMPD1):c.1091+10G>A	rs148067213	0.00033
NM_000543.5(SMPD1):c.1599G>A (p.Pro533=)	rs552841217	0.00004

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