Variants in gene ANO10 with conflicting interpretations "pathogenic" and "likely pathogenic"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_018075.5(ANO10):c.337+1G>A	rs765592794	0.00003
NM_018075.5(ANO10):c.1163-9A>G	rs1368543726	0.00001
NM_018075.5(ANO10):c.124A>T (p.Lys42Ter)	rs768831597	0.00001
NM_018075.5(ANO10):c.289del (p.Thr96_Met97insTer)	rs772345347	0.00001
NM_018075.5(ANO10):c.2T>C (p.Met1Thr)	rs531656357	0.00001
NM_018075.5(ANO10):c.338-2A>G	rs761765455	0.00001
NM_018075.5(ANO10):c.1009T>G (p.Phe337Val)	rs1227163239
NM_018075.5(ANO10):c.1218+1G>C
NM_018075.5(ANO10):c.132dup (p.Asp45fs)	rs540331226
NM_018075.5(ANO10):c.1476+1G>T	rs761213683
NM_018075.5(ANO10):c.1760C>G (p.Ser587Ter)
NM_018075.5(ANO10):c.472+1G>T

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