List of variants in gene combination ANK1, LOC126860369 reported as likely pathogenic for hematologic disorder

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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)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000037.4(ANK1):c.1702-2A>G	rs1554567249
NM_000037.4(ANK1):c.1709del (p.Leu570fs)
NM_000037.4(ANK1):c.1779_1800+1dup
NM_000037.4(ANK1):c.1781_1794del (p.Ser594fs)	rs2150631832
NM_000037.4(ANK1):c.1784dup (p.His596fs)

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