List of variants in gene SLC17A5 reported as likely benign 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_012434.5(SLC17A5):c.613+184C>T	rs16883994	0.01343
NM_012434.5(SLC17A5):c.526-268G>A	rs116972787	0.00793
NM_012434.5(SLC17A5):c.1351-23G>A	rs147885477	0.00359
NM_012434.5(SLC17A5):c.1260-69_1260-68del	rs11349241
NM_012434.5(SLC17A5):c.1351-76del	rs145705821

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