List of variants in gene SLC6A17 reported as uncertain significance 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.1174G>A (p.Val392Ile)	rs114452357	0.00117
NM_001010898.4(SLC6A17):c.1723G>A (p.Val575Met)	rs143189177	0.00022
NM_001010898.4(SLC6A17):c.1105G>A (p.Glu369Lys)	rs149884117	0.00010
NM_001010898.4(SLC6A17):c.824G>A (p.Arg275Gln)	rs147200498	0.00007
NM_001010898.4(SLC6A17):c.489G>C (p.Trp163Cys)	rs1054854634	0.00001
NM_001010898.4(SLC6A17):c.896G>A (p.Arg299Gln)	rs750138241	0.00001
NM_001010898.4(SLC6A17):c.2018C>A (p.Thr673Asn)	rs2100954694

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