List of variants in gene SLC17A5 reported as uncertain significance by GeneDx

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_012434.5(SLC17A5):c.899C>T (p.Ser300Phe)	rs142553916	0.00131
NM_012434.5(SLC17A5):c.1177G>A (p.Val393Ile)	rs140060360	0.00037
NM_012434.5(SLC17A5):c.1046C>T (p.Ala349Val)	rs2533429385
NM_012434.5(SLC17A5):c.1220C>T (p.Ser407Phe)	rs1265357673
NM_012434.5(SLC17A5):c.431T>G (p.Leu144Arg)
NM_012434.5(SLC17A5):c.653G>A (p.Gly218Glu)

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