List of variants in gene SLC22A5 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_003060.4(SLC22A5):c.*843T>C	rs274548	0.74357
NM_003060.4(SLC22A5):c.*1340A>T	rs274547	0.74351
NM_003060.4(SLC22A5):c.959_960insC	rs144261584	0.73243
NM_003060.4(SLC22A5):c.285T>C (p.Leu95=)	rs2631365	0.42203
NM_003060.4(SLC22A5):c.807A>G (p.Leu269=)	rs274558	0.39440
NM_003060.4(SLC22A5):c.824+13T>C	rs274557	0.39418
NM_003060.4(SLC22A5):c.*47C>T	rs1045020	0.09512
NM_003060.4(SLC22A5):c.*92del	rs142209594
NM_003060.4(SLC22A5):c.652+6=	rs4551059

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