ClinVar Miner

List of variants in gene ANK2 reported as uncertain significance for Cardiomyopathy

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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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001148.6(ANK2):c.4310C>T (p.Thr1437Met)	rs142534126	0.00018
NM_001148.6(ANK2):c.9657T>G (p.Ser3219Arg)	rs953435984	0.00001

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