List of variants reported as pathogenic for severe combined immunodeficiency due to DCLRE1C deficiency by Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001033855.3(DCLRE1C):c.1299_1306del (p.Gly434fs)
NM_001033855.3(DCLRE1C):c.1299_1306dup (p.Cys436Ter)	rs2131778656
NM_001374828.1(ARID1B):c.5636_5639del (p.Glu1879fs)	rs1583513256
NM_001374828.1(ARID1B):c.5979_5982del (p.Lys1994fs)

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