Variants in gene ANO10 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_018075.5(ANO10):c.980A>G (p.Tyr327Cys)	rs146569520	0.00359
NM_018075.5(ANO10):c.88G>C (p.Glu30Gln)	rs147605535	0.00085
NM_018075.5(ANO10):c.566G>A (p.Arg189Gln)	rs148873732	0.00056
NM_018075.5(ANO10):c.1843G>A (p.Asp615Asn)	rs138000380	0.00035
NM_018075.5(ANO10):c.397G>A (p.Glu133Lys)	rs571983239	0.00008
NM_018075.5(ANO10):c.1559C>T (p.Ala520Val)	rs150026260	0.00003
NM_018075.5(ANO10):c.1137T>C (p.Tyr379=)
NM_018075.5(ANO10):c.1798-12_1798-9del	rs545954936
NM_018075.5(ANO10):c.45C>T (p.Phe15=)
NM_018075.5(ANO10):c.488C>T (p.Thr163Met)
NM_018075.5(ANO10):c.946C>T (p.Leu316=)

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