List of variants in gene DNMT3A reported as likely pathogenic for See cases

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_022552.5(DNMT3A):c.1792C>T (p.Arg598Ter)	rs568207978	0.00002
NM_022552.5(DNMT3A):c.1490G>T (p.Cys497Phe)	rs779323387
NM_022552.5(DNMT3A):c.1585G>A (p.Asp529Asn)

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