List of variants in gene ANO5 reported as uncertain significance by Institute of Human Genetics, University of Wuerzburg

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_213599.3(ANO5):c.1362G>A (p.Thr454=)	rs747933251	0.00001
NM_213599.3(ANO5):c.754C>T (p.Leu252Phe)	rs1159326828	0.00001
NM_213599.3(ANO5):c.2030-3_2030-2dup	rs768691315

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