List of variants in gene ABCC9 reported as benign by PreventionGenetics, part of Exact Sciences

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_020297.4(ABCC9):c.1660-43C>A	rs704216	0.99827
NM_020297.4(ABCC9):c.2199-11=	rs697250	0.99814
NM_020297.4(ABCC9):c.1296= (p.Pro432=)	rs10770865	0.99692
NM_020297.4(ABCC9):c.1164+11=	rs4762720	0.98998
NM_020297.4(ABCC9):c.1164+23=	rs4762719	0.98997
NM_020297.4(ABCC9):c.406+38A>C	rs2277405	0.64547
NM_020297.4(ABCC9):c.574-5C>A	rs3759236	0.59559
NM_020297.4(ABCC9):c.2424+9T>C	rs11835804	0.02576
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.1056C>T (p.Tyr352=)	rs149408382	0.00276
NM_020297.4(ABCC9):c.2093-7T>C	rs185235724	0.00261
NM_020297.4(ABCC9):c.1677G>A (p.Ala559=)	rs76458291	0.00193
NM_020297.4(ABCC9):c.2769+28A>C	rs2307024

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