Variants in gene TUBB3 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: 16

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HGVS	dbSNP	gnomAD frequency
NM_006086.4(TUBB3):c.58-49C>T	rs28593634	0.19243
NM_006086.4(TUBB3):c.58-22C>T	rs2302897	0.19080
NM_006086.4(TUBB3):c.1215G>A (p.Glu405=)	rs141064323	0.00809
NM_006086.4(TUBB3):c.702C>T (p.Ser234=)	rs147245174	0.00803
NM_006086.4(TUBB3):c.166+12C>T	rs374561094	0.00048
NM_006086.4(TUBB3):c.1287G>A (p.Thr429=)	rs142238093	0.00046
NM_006086.4(TUBB3):c.357G>A (p.Val119=)	rs34174718	0.00040
NM_006086.4(TUBB3):c.507C>T (p.Val169=)	rs373718068	0.00033
NM_006086.4(TUBB3):c.167-6C>T	rs144873806	0.00031
NM_006086.4(TUBB3):c.666C>T (p.Tyr222=)	rs61743676	0.00021
NM_006086.4(TUBB3):c.278-7T>G	rs199842533	0.00011
NM_006086.4(TUBB3):c.447G>A (p.Thr149=)	rs371662941	0.00006
NM_006086.4(TUBB3):c.330G>A (p.Ala110=)	rs535819460	0.00003
NM_006086.4(TUBB3):c.1336G>A (p.Ala446Thr)	rs369454228	0.00001
NM_006086.4(TUBB3):c.167-21C>G	rs72813449
NM_006086.4(TUBB3):c.167-5C>G	rs147928399

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