List of variants in gene combination ANK1, LOC126860368 reported as likely pathogenic for anemia

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000037.4(ANK1):c.4391-1G>C
NM_000037.4(ANK1):c.4465C>T (p.Gln1489Ter)	rs1187228917
NM_000037.4(ANK1):c.4492_4493del (p.Arg1498fs)
NM_000037.4(ANK1):c.4529del (p.Gln1510fs)

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