List of variants in gene ABCC9 reported as likely benign by CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario

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.2200G>A (p.Val734Ile)	rs61688134	0.00769
NM_020297.4(ABCC9):c.798T>C (p.Asp266=)	rs138356189	0.00113
NM_020297.4(ABCC9):c.1557G>A (p.Glu519=)	rs143346402	0.00029
NM_020297.4(ABCC9):c.1909G>A (p.Val637Ile)	rs113542001	0.00016
NM_020297.4(ABCC9):c.142+10C>A	rs138917284	0.00007
NM_020297.4(ABCC9):c.3357G>A (p.Leu1119=)	rs2287626	0.00003
NM_020297.4(ABCC9):c.3007T>C (p.Leu1003=)	rs138700703	0.00001
NM_020297.4(ABCC9):c.957T>C (p.Ser319=)	rs768245158	0.00001
NM_020297.4(ABCC9):c.1471A>C (p.Arg491=)	rs1948042755
NM_020297.4(ABCC9):c.1521G>A (p.Leu507=)	rs1565470512
NM_020297.4(ABCC9):c.2475G>A (p.Ala825=)	rs587780845
NM_020297.4(ABCC9):c.2799G>A (p.Glu933=)	rs1565735141
NM_020297.4(ABCC9):c.420T>C (p.Tyr140=)	rs397517189
NM_020297.4(ABCC9):c.90C>T (p.Asn30=)	rs1428470419

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