List of variants in gene MAGI2 reported as benign by Genetic Services Laboratory, University of Chicago

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_012301.4(MAGI2):c.4329C>G (p.Pro1443=)	rs13438302	0.29174
NM_012301.4(MAGI2):c.4269G>C (p.Pro1423=)	rs2960452	0.27858
NM_012301.4(MAGI2):c.3915G>A (p.Gln1305=)	rs117054456	0.02550
NM_012301.4(MAGI2):c.1755C>T (p.Pro585=)	rs34937835	0.01550
NM_012301.4(MAGI2):c.531T>C (p.Thr177=)	rs34088845	0.00991
NM_012301.4(MAGI2):c.893A>G (p.Asn298Ser)	rs149573681	0.00511
NM_012301.4(MAGI2):c.2213G>A (p.Arg738Gln)	rs145722885	0.00153

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