List of variants in gene MAGT1 reported as pathogenic by OMIM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_001367916.1(MAGT1):c.313C>T (p.Arg105Ter)	rs387906724
NM_001367916.1(MAGT1):c.459dup (p.Tyr154fs)	rs1603361804
NM_001367916.1(MAGT1):c.502del (p.Arg168fs)	rs1603361795
NM_001367916.1(MAGT1):c.616C>T (p.Arg206Ter)	rs879989957
NM_001367916.1(MAGT1):c.826_826+9del	rs1603361427
NM_001367916.1(MAGT1):c.842T>G (p.Leu281Ter)	rs1569547878
NM_001367916.1(MAGT1):c.895C>T (p.Arg299Ter)	rs1569547876
NM_001367916.1(MAGT1):c.972A>C (p.Lys324Asn)	rs373260156

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