Variants in gene ANO10 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_018075.5(ANO10):c.1843G>A (p.Asp615Asn)	rs138000380	0.00035
NM_018075.5(ANO10):c.512T>C (p.Phe171Ser)	rs373386030	0.00004
NM_018075.5(ANO10):c.132dup (p.Asp45fs)	rs540331226

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