List of variants in gene SLC52A3 reported as 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_033409.4(SLC52A3):c.907A>G (p.Ile303Val)	rs3746802	0.09243
NM_033409.4(SLC52A3):c.240C>T (p.Gly80=)	rs34376836	0.01265
NM_033409.4(SLC52A3):c.600C>T (p.Pro200=)	rs16992990	0.00815
NM_033409.4(SLC52A3):c.833C>T (p.Thr278Met)	rs3746803

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