List of variants in gene SLC5A1 reported as benign by Illumina Laboratory Services, Illumina

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_000343.4(SLC5A1):c.*2257A>G	rs5753868	0.92649
NM_000343.4(SLC5A1):c.*706C>T	rs1056444	0.58787
NM_000343.4(SLC5A1):c.1129+7T>G	rs5998233	0.47147
NM_000343.4(SLC5A1):c.*1804T>C	rs17683807	0.22133
NM_000343.4(SLC5A1):c.*2245C>T	rs9621386	0.14372
NM_000343.4(SLC5A1):c.1845C>G (p.His615Gln)	rs33954001	0.04760
NM_000343.4(SLC5A1):c.1275C>T (p.Ala425=)	rs17683448	0.04560
NM_000343.4(SLC5A1):c.1938C>T (p.Asn646=)	rs33954397	0.04560
NM_000343.4(SLC5A1):c.1231G>A (p.Ala411Thr)	rs17683430	0.04557
NM_000343.4(SLC5A1):c.152A>G (p.Asn51Ser)	rs17683011	0.04555
NM_000343.4(SLC5A1):c.1836A>G (p.Leu612=)	rs17683704	0.04554
NM_000343.4(SLC5A1):c.1899G>A (p.Thr633=)	rs33943816	0.04197
NM_000343.4(SLC5A1):c.*902T>G	rs16989883	0.02647
NM_000343.4(SLC5A1):c.*1508C>A	rs8142324	0.01304
NM_000343.4(SLC5A1):c.*795G>T	rs117904039	0.01237
NM_000343.4(SLC5A1):c.6C>T (p.Asp2=)	rs33973317	0.01145
NM_000343.3(SLC5A1):c.-170C>T	rs142248518	0.01139
NM_000343.4(SLC5A1):c.1666-5T>C	rs33968460	0.01076
NM_000343.4(SLC5A1):c.*2244C>T	rs114700055	0.01052
NM_000343.4(SLC5A1):c.1092C>T (p.Ile364=)	rs33915456	0.00975
NM_000343.4(SLC5A1):c.50T>C (p.Val17Ala)	rs33951240	0.00787
NM_000343.4(SLC5A1):c.1130-9C>T	rs33914280	0.00761
NM_000343.4(SLC5A1):c.*1432G>T	rs28540121	0.00663
NM_000343.4(SLC5A1):c.*2275C>T	rs144145176	0.00438
NM_000343.4(SLC5A1):c.*400C>T	rs117362976	0.00052
NM_000343.4(SLC5A1):c.*771C>T	rs550005508	0.00003
NM_000343.4(SLC5A1):c.*1940G>A	rs117112619

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