List of variants in gene DAG1 reported as benign for hereditary skeletal muscle disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_004393.6(DAG1):c.41C>G (p.Ser14Trp)	rs2131107	0.97526
NM_004393.6(DAG1):c.285+42T>C	rs2329024	0.97521
NM_004393.6(DAG1):c.*250T>C	rs1050088	0.39364
NM_004393.6(DAG1):c.2256C>T (p.His752=)	rs1801143	0.30176
NM_004393.6(DAG1):c.41= (p.Ser14=)	rs1553648360	0.02474
NM_004393.6(DAG1):c.2231G>C (p.Ser744Thr)	rs114357468	0.00947
NM_004393.6(DAG1):c.2271C>T (p.Ala757=)	rs78281659	0.00786
NM_004393.6(DAG1):c.259A>G (p.Ile87Val)	rs116717961	0.00640
NM_004393.6(DAG1):c.1701C>T (p.Ser567=)	rs142579425	0.00456
NM_004393.6(DAG1):c.1233G>A (p.Val411=)	rs145765079	0.00249
NM_004393.6(DAG1):c.607A>T (p.Thr203Ser)	rs200094365	0.00108
NM_004393.6(DAG1):c.2520T>C (p.Thr840=)	rs149564053	0.00074
NM_004393.6(DAG1):c.331G>A (p.Asp111Asn)	rs117209107	0.00072
NM_004393.6(DAG1):c.927C>T (p.Arg309=)	rs551679833	0.00006
NM_004393.6(DAG1):c.384G>T (p.Val128=)	rs143829263

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