List of variants in gene MAGI2 reported as uncertain significance by GeneDx

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_012301.4(MAGI2):c.2131C>A (p.Pro711Thr)	rs144078604	0.00029
NM_012301.4(MAGI2):c.4255C>G (p.Pro1419Ala)	rs1584845985	0.00004
NM_012301.4(MAGI2):c.3802T>G (p.Ser1268Ala)	rs767664742	0.00001
NM_012301.4(MAGI2):c.1691G>A (p.Arg564Gln)
NM_012301.4(MAGI2):c.1940T>C (p.Val647Ala)
NM_012301.4(MAGI2):c.2120G>T (p.Ser707Ile)	rs2535284648
NM_012301.4(MAGI2):c.2131C>T (p.Pro711Ser)
NM_012301.4(MAGI2):c.2483T>C (p.Val828Ala)	rs2485790641
NM_012301.4(MAGI2):c.2616C>G (p.Asn872Lys)	rs148005928
NM_012301.4(MAGI2):c.3123G>A (p.Gln1041=)	rs1418143177

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