List of variants in gene DAG1 reported as uncertain significance by GeneDx

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: 16

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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	0.00024
NM_004393.6(DAG1):c.1306A>G (p.Thr436Ala)	rs149838438	0.00009
NM_004393.6(DAG1):c.1708G>A (p.Val570Met)	rs370669533	0.00006
NM_004393.6(DAG1):c.244A>G (p.Ile82Val)	rs141706514	0.00006
NM_004393.6(DAG1):c.829G>A (p.Val277Ile)	rs375892170	0.00006
NM_004393.6(DAG1):c.1283G>A (p.Arg428Gln)	rs780793711	0.00004
NM_004393.6(DAG1):c.2123C>T (p.Thr708Met)	rs758254304	0.00004
NM_004393.6(DAG1):c.559C>T (p.Pro187Ser)	rs145540662	0.00004
NM_004393.6(DAG1):c.1186A>G (p.Thr396Ala)	rs779846682	0.00002
NM_004393.6(DAG1):c.1210A>G (p.Thr404Ala)	rs769229834	0.00002
NM_004393.6(DAG1):c.268A>C (p.Ser90Arg)	rs140454570	0.00001
NM_004393.6(DAG1):c.1442G>C (p.Arg481Pro)	rs1256677839
NM_004393.6(DAG1):c.1591_1593del (p.Thr531del)	rs1553653146
NM_004393.6(DAG1):c.2270C>T (p.Ala757Val)	rs1131691522
NM_004393.6(DAG1):c.2629G>A (p.Gly877Ser)	rs2107959292

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