List of variants in gene ABCC9 reported as benign by Ambry Genetics

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_020297.4(ABCC9):c.1296= (p.Pro432=)	rs10770865	0.99692
NM_020297.4(ABCC9):c.574-5C>A	rs3759236	0.59559
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.2200G>A (p.Val734Ile)	rs61688134	0.00769
NM_020297.4(ABCC9):c.2631G>A (p.Thr877=)	rs139408145	0.00386
NM_020297.4(ABCC9):c.2523C>T (p.Ala841=)	rs144537241	0.00345
NM_020297.4(ABCC9):c.1677G>A (p.Ala559=)	rs76458291	0.00193
NM_020297.4(ABCC9):c.2238-1G>A	rs141281214	0.00056
NM_020297.4(ABCC9):c.3267G>A (p.Leu1089=)	rs780998911	0.00009
NM_020297.4(ABCC9):c.1988G>A (p.Arg663His)	rs141999048	0.00006
NM_020297.4(ABCC9):c.1993G>A (p.Ala665Thr)	rs200891785	0.00005
NM_020297.4(ABCC9):c.2763A>G (p.Leu921=)	rs760466255

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