Variants in gene GAN with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (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: 8

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HGVS	dbSNP	gnomAD frequency
NM_022041.4(GAN):c.1293C>T (p.Tyr431=)	rs2608555	0.21491
NM_022041.4(GAN):c.1239C>T (p.Ile413=)	rs61740238	0.00609
NM_022041.4(GAN):c.1684C>G (p.Pro562Ala)	rs79901179	0.00388
NM_022041.4(GAN):c.1182C>T (p.Tyr394=)	rs150102659	0.00357
NM_022041.4(GAN):c.1502+11A>G	rs143413333	0.00263
NM_022041.4(GAN):c.1612+12A>G	rs150344737	0.00135
NM_022041.4(GAN):c.1162C>T (p.Leu388=)	rs73589395	0.00103
NM_022041.4(GAN):c.283-20T>C	rs371984923	0.00093

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