List of variants reported as likely pathogenic for X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia by Labcorp Genetics (formerly Invitae), Labcorp

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NC_000023.10:g.(?_77084697)_(77131114_?)del
NC_000023.10:g.(?_77086282)_(77131114_?)dup
NC_000023.10:g.(?_77112986)_(77112986_?)del
NM_001367916.1(MAGT1):c.399del (p.Met133fs)	rs1603361811
NM_001367916.1(MAGT1):c.673-1G>A	rs2149017840
NM_001367916.1(MAGT1):c.762+1G>A
NM_001367916.1(MAGT1):c.827-1_838del	rs1603359848

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