ClinVar Miner

List of variants in gene SLC1A3 reported as likely benign for Inborn genetic diseases

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_004172.5(SLC1A3):c.1074C>T (p.Thr358=)	rs147973032	0.00068
NM_004172.5(SLC1A3):c.1589A>G (p.Asn530Ser)	rs753745170	0.00004

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