List of variants in gene ARSL reported as benign by Genetic Services Laboratory, University of Chicago

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000047.3(ARSL):c.1270G>A (p.Gly424Ser)	rs35143646	0.50841
NM_000047.3(ARSL):c.1692C>T (p.Asn564=)	rs11222	0.47884
NM_000047.3(ARSL):c.78A>G (p.Ala26=)	rs35718384	0.07015
NM_000047.3(ARSL):c.786G>A (p.Thr262=)	rs17325750	0.05921
NM_000047.3(ARSL):c.1728G>A (p.Pro576=)	rs11055	0.05776
NM_000047.3(ARSL):c.549C>T (p.Arg183=)	rs5982618	0.03335
NM_000047.3(ARSL):c.157A>G (p.Ile53Val)	rs61733256	0.02854
NM_000047.3(ARSL):c.548G>A (p.Arg183His)	rs34412194	0.01378
NM_000047.3(ARSL):c.867G>A (p.Gly289=)	rs587783181	0.00005
NM_000047.3(ARSL):c.495T>G (p.His165Gln)	rs35274634

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