ClinVar Miner

List of variants in gene SLC1A3 reported as uncertain significance 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_004172.5(SLC1A3):c.955G>A (p.Val319Met)	rs753136358	0.00002
NM_004172.5(SLC1A3):c.139C>G (p.Arg47Gly)	rs2477871926

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