Variants in gene TUBA1A with conflicting interpretations "likely pathogenic" and "uncertain significance"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_006009.4(TUBA1A):c.188C>T (p.Pro63Leu)	rs2121247772
NM_006009.4(TUBA1A):c.26T>C (p.Val9Ala)	rs1565627795
NM_006009.4(TUBA1A):c.362G>A (p.Arg121Gln)	rs2121246284
NM_006009.4(TUBA1A):c.518C>T (p.Pro173Leu)	rs1565627304
NM_006009.4(TUBA1A):c.521C>T (p.Ala174Val)	rs587784489
NM_006009.4(TUBA1A):c.528G>C (p.Gln176His)
NM_006009.4(TUBA1A):c.791G>A (p.Arg264His)	rs886043627

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