List of variants in gene SLC5A1 reported as likely benign by Fulgent Genetics, Fulgent Genetics

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000343.4(SLC5A1):c.1092C>T (p.Ile364=)	rs33915456	0.00975
NM_000343.4(SLC5A1):c.1200C>T (p.Ser400=)	rs142046439	0.00027
NM_000343.4(SLC5A1):c.1752T>G (p.Pro584=)	rs149362007	0.00024
NM_000343.4(SLC5A1):c.208-8G>A	rs199783226	0.00016
NM_000343.4(SLC5A1):c.30C>T (p.Thr10=)	rs750528703	0.00001
NM_000343.4(SLC5A1):c.886-10T>C	rs201709042	0.00001
NM_000343.4(SLC5A1):c.1772-6G>A	rs201685531
NM_000343.4(SLC5A1):c.373-7del	rs778194598
NM_000343.4(SLC5A1):c.584-6G>A	rs200525887

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