List of variants in gene SLC1A3 reported as uncertain significance by Genome-Nilou Lab

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_004172.5(SLC1A3):c.1496G>A (p.Arg499Gln)	rs138085358	0.00007
NM_004172.5(SLC1A3):c.510C>G (p.Phe170Leu)	rs774420370	0.00003
NM_004172.5(SLC1A3):c.212A>G (p.Tyr71Cys)	rs573483474	0.00002
NM_004172.5(SLC1A3):c.28A>G (p.Lys10Glu)	rs754763002	0.00002
NM_004172.5(SLC1A3):c.625C>G (p.Leu209Val)	rs146815724

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