List of variants in gene combination ANK1, LOC124153154 reported as uncertain significance for anemia

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000037.4(ANK1):c.447G>T (p.Ala149=)	rs140550365	0.00025
NM_000037.4(ANK1):c.499G>C (p.Gly167Arg)	rs201024919	0.00021
NM_000037.4(ANK1):c.563C>T (p.Thr188Met)	rs146346710	0.00004
NM_000037.4(ANK1):c.455T>C (p.Leu152Pro)

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