ClinVar Miner

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

Included ClinVar conditions (2):

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000037.4(ANK1):c.450A>G (p.Val150=)	rs6982971	0.04455
NM_000037.4(ANK1):c.489C>T (p.Leu163=)	rs34173100	0.01106

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