List of variants in gene ANO1 reported as likely benign by Ambry Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_018043.7(ANO1):c.1908G>A (p.Pro636=)	rs375335468	0.00040
NM_018043.7(ANO1):c.2377A>G (p.Ile793Val)	rs368994897	0.00014
NM_018043.7(ANO1):c.1098C>T (p.Ser366=)
NM_018043.7(ANO1):c.2117G>A (p.Cys706Tyr)
NM_018043.7(ANO1):c.919C>T (p.Arg307Cys)

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