List of variants in gene ANK2 reported as likely pathogenic by Medical Research Institute, Tokyo Medical and Dental University

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_001148.6(ANK2):c.2474C>T (p.Thr825Ile)	rs786205420
NM_001148.6(ANK2):c.4876A>G (p.Lys1626Glu)	rs755287627
NM_001148.6(ANK2):c.8123T>C (p.Val2708Ala)	rs796052198

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