List of variants in gene SLC22A5 reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 13

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HGVS	dbSNP	gnomAD frequency
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.652+77A>G	rs274559	0.39418
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.1268-34A>G	rs11568515	0.03088
NM_003060.4(SLC22A5):c.1587-38A>C	rs11568523	0.03088
NM_003060.4(SLC22A5):c.393+17G>A	rs11568522	0.02888
NM_003060.4(SLC22A5):c.1645C>T (p.Pro549Ser)	rs11568525	0.02345
NM_003060.4(SLC22A5):c.430C>T (p.Leu144Phe)	rs10040427	0.02340
NM_003060.4(SLC22A5):c.1463G>A (p.Arg488His)	rs28383481	0.00347
NM_003060.4(SLC22A5):c.1268-38del	rs11568517
NM_003060.4(SLC22A5):c.652+6=	rs4551059

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