List of variants in gene SLC1A2 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_004171.4(SLC1A2):c.1368C>T (p.Ala456=)	rs16927239	0.00081
NM_004171.4(SLC1A2):c.-4del	rs755227278	0.00030
NM_004171.4(SLC1A2):c.1317G>A (p.Ala439=)	rs149714933	0.00016
NM_004171.4(SLC1A2):c.1335C>T (p.Ala445=)	rs139804773	0.00013
NM_004171.4(SLC1A2):c.669G>A (p.Pro223=)	rs372812420	0.00005
NM_004171.4(SLC1A2):c.1309G>A (p.Val437Ile)	rs374090482	0.00004
NM_004171.4(SLC1A2):c.580A>G (p.Lys194Glu)	rs150854080	0.00004
NM_004171.4(SLC1A2):c.1314C>T (p.Gly438=)	rs760683483	0.00002
NM_004171.4(SLC1A2):c.159T>A (p.Gly53=)
NM_004171.4(SLC1A2):c.1653+24C>T
NM_004171.4(SLC1A2):c.612G>A (p.Glu204=)

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