List of variants in gene ANK2 reported as likely pathogenic for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001148.6(ANK2):c.11859+2T>G
NM_001148.6(ANK2):c.2575G>T (p.Gly859Ter)	rs2079824761
NM_001148.6(ANK2):c.2944C>T (p.Arg982Ter)	rs1588354762
NM_001148.6(ANK2):c.3201dup (p.Pro1068fs)
NM_001148.6(ANK2):c.3490_3493del (p.Ile1164fs)	rs1588487990
NM_001148.6(ANK2):c.6757_6761del (p.Lys2252_Lys2253insTer)
NM_001148.6(ANK2):c.85-56996T>C	rs2154369391

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