List of variants in gene ABCC9 reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 18

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HGVS	dbSNP	gnomAD frequency
NM_020297.4(ABCC9):c.2424+9T>C	rs11835804	0.02576
NM_020297.4(ABCC9):c.1848C>T (p.Asp616=)	rs61001398	0.01493
NM_020297.4(ABCC9):c.3321C>T (p.Ile1107=)	rs35404804	0.01226
NM_020297.4(ABCC9):c.789C>T (p.Cys263=)	rs58386780	0.01183
NM_020297.4(ABCC9):c.2200G>A (p.Val734Ile)	rs61688134	0.00769
NM_020297.4(ABCC9):c.3409G>A (p.Val1137Ile)	rs147895473	0.00739
NM_020297.4(ABCC9):c.2644-19G>A	rs73254534	0.00507
NM_020297.4(ABCC9):c.285-16G>A	rs144825585	0.00448
NM_020297.4(ABCC9):c.2523C>T (p.Ala841=)	rs144537241	0.00345
NM_020297.4(ABCC9):c.2093-7T>C	rs185235724	0.00261
NM_020297.4(ABCC9):c.407-14C>A	rs201279882	0.00248
NM_020297.4(ABCC9):c.3768T>C (p.Leu1256=)	rs150303433	0.00209
NM_020297.4(ABCC9):c.1677G>A (p.Ala559=)	rs76458291	0.00193
NM_020297.4(ABCC9):c.924T>C (p.Asp308=)	rs139127928	0.00140
NM_020297.4(ABCC9):c.3339T>G (p.Ser1113=)	rs138280089	0.00031
NM_020297.4(ABCC9):c.2644-11G>A	rs61926078
NM_020297.4(ABCC9):c.817-18del	rs199947733
NM_020297.4(ABCC9):c.817-7del	rs193922684

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