List of variants in gene SLC22A5 reported as likely benign for not specified

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_003060.4(SLC22A5):c.1451-16G>A	rs140988771	0.00371
NM_003060.4(SLC22A5):c.1463G>A (p.Arg488His)	rs28383481	0.00347
NM_003060.4(SLC22A5):c.1380C>T (p.Asn460=)	rs149521997	0.00079
NM_003060.4(SLC22A5):c.-26G>A	rs369724970	0.00023
NM_003060.4(SLC22A5):c.1377A>G (p.Arg459=)	rs142264458	0.00018
NM_003060.4(SLC22A5):c.246C>T (p.Arg82=)	rs377767448	0.00004
NM_003060.4(SLC22A5):c.523G>A (p.Val175Met)	rs781721860	0.00003
NM_003060.4(SLC22A5):c.1185A>G (p.Gln395=)	rs916795176	0.00002
NM_003060.4(SLC22A5):c.573G>T (p.Lys191Asn)	rs765204844	0.00002
NM_003060.4(SLC22A5):c.1125C>T (p.Asn375=)	rs202219455	0.00001
NM_003060.4(SLC22A5):c.405G>A (p.Val135=)	rs777083211	0.00001
NM_003060.4(SLC22A5):c.1080G>T (p.Gly360=)	rs139508856
NM_003060.4(SLC22A5):c.1170C>G (p.Ala390=)	rs774368158
NM_003060.4(SLC22A5):c.394-18C>G	rs200136788

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