List of variants in gene ARSL 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: 12

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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.23+687G>A	rs61733257	0.02344
NM_000047.3(ARSL):c.1408G>C (p.Asp470His)	rs61743737	0.00143
NM_000047.3(ARSL):c.1289+9C>T	rs375386476	0.00136
NM_000047.3(ARSL):c.1386C>T (p.His462=)	rs183018622	0.00013
NM_000047.3(ARSL):c.-14GA[3]	rs200332753

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