List of variants in gene ANO5 reported as likely pathogenic by Mayo Clinic Laboratories, Mayo Clinic

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_213599.3(ANO5):c.1640G>A (p.Arg547Gln)	rs139618850	0.00015
NM_213599.3(ANO5):c.172C>T (p.Arg58Trp)	rs201725369	0.00014
NM_213599.3(ANO5):c.1965G>A (p.Trp655Ter)	rs760137559
NM_213599.3(ANO5):c.2411G>C (p.Cys804Ser)	rs1233836740

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