List of variants in gene SLC1A3 reported as likely 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_004172.5(SLC1A3):c.1489T>C (p.Leu497=)	rs150357327	0.00272
NM_004172.5(SLC1A3):c.15T>C (p.Asn5=)	rs143791614	0.00063
NM_004172.5(SLC1A3):c.676C>G (p.Arg226Gly)	rs201069745	0.00016
NM_004172.5(SLC1A3):c.1449C>T (p.Asn483=)	rs758716513	0.00013

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