ClinVar Miner

List of variants reported as likely pathogenic for megaloblastic anemia by Illumina Laboratory Services, Illumina

Included ClinVar conditions (12):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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_001081.4(CUBN):c.348+2T>C	rs146047781	0.00012
NM_001081.4(CUBN):c.5913_5916del (p.Thr1972fs)	rs765301342

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