List of variants in gene SLC6A17 reported as likely benign by Genetic Services Laboratory, University of Chicago

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001010898.4(SLC6A17):c.525G>A (p.Pro175=)	rs142901935	0.00138
NM_001010898.4(SLC6A17):c.286+10A>G	rs187996451	0.00119
NM_001010898.4(SLC6A17):c.696C>T (p.Leu232=)	rs373414163	0.00026
NM_001010898.4(SLC6A17):c.1287C>T (p.Asp429=)	rs151152223	0.00016
NM_001010898.4(SLC6A17):c.1941C>G (p.Gly647=)	rs376648268	0.00001
NM_001010898.4(SLC6A17):c.303C>A (p.Pro101=)	rs746434391	0.00001
NM_001010898.4(SLC6A17):c.1806C>T (p.Ile602=)	rs201061830

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