List of variants in gene ABCC9 reported as likely benign for cardiac rhythm disease

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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: 9

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HGVS	dbSNP	gnomAD frequency
NM_020297.4(ABCC9):c.1848C>T (p.Asp616=)	rs61001398	0.01493
NM_020297.4(ABCC9):c.1887G>T (p.Glu629Asp)	rs150036969	0.00032
NM_020297.4(ABCC9):c.3315+17C>T	rs200692327	0.00023
NM_020297.4(ABCC9):c.2339+13A>G	rs189255166	0.00012
NM_020297.4(ABCC9):c.142+10C>A	rs138917284	0.00007
NM_020297.4(ABCC9):c.3462G>A (p.Arg1154=)	rs1336342134	0.00002
NM_020297.4(ABCC9):c.1671C>A (p.Thr557=)	rs746467455	0.00001
NM_020297.4(ABCC9):c.2238-17del	rs4148670
NM_020297.4(ABCC9):c.4450-6_4450-5del	rs4148680

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