List of variants in gene combination ANK1, LOC124153154 reported as likely benign for anemia

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000037.4(ANK1):c.489C>T (p.Leu163=)	rs34173100	0.01106
NM_000037.4(ANK1):c.447G>T (p.Ala149=)	rs140550365	0.00025
NM_000037.4(ANK1):c.528C>T (p.Ala176=)	rs544906793	0.00018
NM_000037.4(ANK1):c.483G>A (p.Ala161=)	rs200639644	0.00009

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