List of variants in gene DAG1 reported as uncertain significance by Breakthrough Genomics, Breakthrough Genomics

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_004393.6(DAG1):c.1022C>T (p.Thr341Ile)	rs148759919	0.00048
NM_004393.6(DAG1):c.920C>G (p.Pro307Arg)	rs374092106	0.00022
NM_004393.6(DAG1):c.1673G>T (p.Ser558Ile)	rs746984955	0.00001
NM_004393.6(DAG1):c.2647A>G (p.Met883Val)	rs754908618	0.00001
NM_004393.6(DAG1):c.2561G>A (p.Arg854Gln)	rs199933395

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