List of variants in gene ABAT reported as benign by Mayo Clinic Laboratories, Mayo Clinic

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_020686.6(ABAT):c.167A>G (p.Gln56Arg)	rs1731017	0.53047
NM_020686.6(ABAT):c.169-5T>C	rs1641010	0.49394
NM_020686.6(ABAT):c.1381+9T>C	rs1079348	0.33159
NM_020686.6(ABAT):c.984C>A (p.Val328=)	rs1641022	0.32625
NM_020686.6(ABAT):c.309C>T (p.Val103=)	rs2229157	0.09544
NM_020686.6(ABAT):c.1270-4A>G	rs12447235	0.07354
NM_020686.6(ABAT):c.129G>A (p.Gly43=)	rs2228081	0.03085
NM_020686.6(ABAT):c.1147C>T (p.Leu383=)	rs2229158	0.02911

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