Variants in gene ANK1 with conflicting interpretations "likely pathogenic" and "pathogenic"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 12

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HGVS	dbSNP	gnomAD frequency
NM_000037.4(ANK1):c.5497C>T (p.Arg1833Ter)	rs137852831	0.00001
NM_000037.4(ANK1):c.1801-17G>A	rs786205243
NM_000037.4(ANK1):c.2029C>T (p.Gln677Ter)	rs1563502820
NM_000037.4(ANK1):c.2394_2397del (p.Ser799fs)	rs2150605978
NM_000037.4(ANK1):c.3325C>T (p.Gln1109Ter)	rs2150593157
NM_000037.4(ANK1):c.3533-2A>G
NM_000037.4(ANK1):c.3893_3894del (p.Ser1298fs)
NM_000037.4(ANK1):c.3984+2T>C	rs1818974494
NM_000037.4(ANK1):c.4000C>T (p.Arg1334Ter)	rs1172677213
NM_000037.4(ANK1):c.409C>T (p.Gln137Ter)	rs2150661792
NM_000037.4(ANK1):c.5197C>T (p.Gln1733Ter)
NM_000037.4(ANK1):c.6dup (p.Tyr3fs)

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