List of variants in gene SLC1A3 reported as likely benign by Genome Diagnostics Laboratory, University Medical Center Utrecht

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.15T>C (p.Asn5=)	rs143791614	0.00063
NM_004172.5(SLC1A3):c.320-7C>T	rs200867287	0.00063
NM_004172.5(SLC1A3):c.648T>C (p.Asn216=)	rs139342707	0.00045
NM_004172.5(SLC1A3):c.1425-8G>C	rs202233020	0.00016

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