ClinVar Miner

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

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 5
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HGVS dbSNP gnomAD frequency
NC_000023.10:g.(?_77084697)_(77131114_?)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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