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

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_018075.5(ANO10):c.1385G>A (p.Arg462Gln)	rs3772165	0.58882
NM_018075.5(ANO10):c.1066A>G (p.Ser356Gly)	rs56389778	0.05750
NM_018075.5(ANO10):c.1682C>T (p.Thr561Met)	rs17409162	0.04859
NM_018075.5(ANO10):c.788G>A (p.Arg263His)	rs41289586	0.01896
NM_018075.5(ANO10):c.74A>C (p.Gln25Pro)	rs112040665	0.01413
NM_018075.5(ANO10):c.1915-5816C>A	rs146629436	0.00245
NM_018075.5(ANO10):c.963C>T (p.Phe321=)	rs149196477	0.00097
NM_018075.5(ANO10):c.1914+3G>A	rs113187031	0.00068
NM_018075.5(ANO10):c.1219-23dup	rs367784953
NM_018075.5(ANO10):c.159A>G (p.Arg53=)	rs533186096
NM_018075.5(ANO10):c.1683G>C (p.Thr561=)	rs141040660

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