List of variants in gene ABCC9 reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

Minimum submission review status:		Collection method:
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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: 13

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HGVS	dbSNP	gnomAD frequency
NM_020297.4(ABCC9):c.2050G>A (p.Gly684Ser)	rs148174226	0.00039
NM_020297.4(ABCC9):c.1887G>T (p.Glu629Asp)	rs150036969	0.00032
NM_020297.4(ABCC9):c.305T>C (p.Leu102Pro)	rs374659816	0.00029
NM_020297.4(ABCC9):c.4512+690C>T	rs397517191	0.00017
NM_020297.4(ABCC9):c.4344T>C (p.Asn1448=)	rs146782703	0.00009
NM_020297.4(ABCC9):c.1551T>C (p.Ser517=)	rs996266050	0.00004
NM_020297.4(ABCC9):c.2004G>A (p.Glu668=)	rs751485829	0.00002
NM_020297.4(ABCC9):c.1194C>T (p.Leu398=)	rs1430745818	0.00001
NM_020297.4(ABCC9):c.957T>C (p.Ser319=)	rs768245158	0.00001
NM_020297.4(ABCC9):c.1619-20C>A	rs1357942810
NM_020297.4(ABCC9):c.1629T>C (p.Asn543=)
NM_020297.4(ABCC9):c.3063G>A (p.Glu1021=)	rs1555187269
NM_020297.4(ABCC9):c.771A>C (p.Ala257=)

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