List of variants in gene combination ANK1, LOC130000286 reported as likely benign 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000037.4(ANK1):c.2352C>T (p.Asp784=)	rs751238125	0.00002
NM_000037.4(ANK1):c.2370G>T (p.Thr790=)	rs540304535	0.00001

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