Variants in gene MAGI2 with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 10

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HGVS	dbSNP	gnomAD frequency
NM_012301.4(MAGI2):c.2142G>A (p.Pro714=)	rs144574076	0.00156
NM_012301.4(MAGI2):c.219C>T (p.Pro73=)	rs148240352	0.00143
NM_012301.4(MAGI2):c.2454C>T (p.Arg818=)	rs148580718	0.00081
NM_012301.4(MAGI2):c.3706+5G>A	rs188293910	0.00060
NM_012301.4(MAGI2):c.2131C>A (p.Pro711Thr)	rs144078604	0.00031
NM_012301.4(MAGI2):c.411G>A (p.Thr137=)	rs149568072	0.00024
NM_012301.4(MAGI2):c.1737C>T (p.Asp579=)	rs142555732	0.00009
NM_012301.4(MAGI2):c.1713C>T (p.Ser571=)	rs587780386	0.00003
NM_012301.4(MAGI2):c.878C>T (p.Thr293Ile)	rs587780389	0.00002
NM_012301.4(MAGI2):c.1425T>C (p.Tyr475=)	rs148086431	0.00001

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