List of variants in gene MAGI2 reported as benign by Athena Diagnostics Inc

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_012301.4(MAGI2):c.3357A>G (p.Leu1119=)	rs2074641	0.86492
NM_012301.4(MAGI2):c.3213G>A (p.Ser1071=)	rs7812015	0.86488
NM_012301.4(MAGI2):c.1014G>A (p.Lys338=)	rs3735442	0.33029
NM_012301.4(MAGI2):c.2784T>C (p.Asn928=)	rs1009524	0.11193
NM_012301.4(MAGI2):c.3915G>A (p.Gln1305=)	rs117054456	0.02550
NM_012301.4(MAGI2):c.531T>C (p.Thr177=)	rs34088845	0.00991
NM_012301.4(MAGI2):c.2379C>T (p.Leu793=)	rs73703715	0.00966
NM_012301.4(MAGI2):c.2329T>C (p.Leu777=)	rs76346657	0.00722
NM_012301.4(MAGI2):c.219C>T (p.Pro73=)	rs148240352	0.00143

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