ClinVar Miner

List of variants in gene MAGT1 reported as benign for X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_001367916.1(MAGT1):c.673-16T>C rs140957691 0.03076
NM_001367916.1(MAGT1):c.651T>A (p.Thr217=) rs61732679 0.01635
NM_001367916.1(MAGT1):c.932T>G (p.Val311Gly) rs145245774 0.00119
NM_032121.5(MAGT1):c.67G>A (p.Val23Ile) rs182757967 0.00049
NM_032121.5(MAGT1):c.3G>A (p.Met1Ile) rs185325713 0.00039
NM_001367916.1(MAGT1):c.103-17C>T rs782234408 0.00024
NM_001367916.1(MAGT1):c.532-12C>G rs781848524 0.00015
NM_001367916.1(MAGT1):c.511G>A (p.Ala171Thr) rs141774769 0.00014
NM_001367916.1(MAGT1):c.207G>A (p.Pro69=) rs782428049 0.00012
NM_001367916.1(MAGT1):c.192T>C (p.Leu64=) rs189513206 0.00008
NM_001367916.1(MAGT1):c.763-14T>G rs782170645 0.00008
NM_001367916.1(MAGT1):c.390+6A>G rs782066955 0.00007
NM_001367916.1(MAGT1):c.272+13A>G rs782567093 0.00004
NM_001367916.1(MAGT1):c.342A>T (p.Ile114=) rs368934480 0.00003
NM_001367916.1(MAGT1):c.272+8C>T rs373819700 0.00002
NM_001367916.1(MAGT1):c.771C>T (p.Ile257=) rs782533209 0.00002
NM_001367916.1(MAGT1):c.273-18G>A
NM_001367916.1(MAGT1):c.574T>C (p.Leu192=)
NM_001367916.1(MAGT1):c.702A>G (p.Gln234=)
NM_001367916.1(MAGT1):c.827-16A>G
NM_032121.5(MAGT1):c.44C>T (p.Thr15Ile)

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