List of variants in gene SLC22A8 reported as likely benign for not specified

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_004254.4(SLC22A8):c.742G>A (p.Val248Ile)	rs146180971	0.00009
NM_004254.4(SLC22A8):c.127G>A (p.Ala43Thr)	rs200181297	0.00003
NM_004254.4(SLC22A8):c.44A>G (p.His15Arg)	rs1325562303	0.00002
NM_004254.4(SLC22A8):c.614G>A (p.Arg205Gln)

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