ClinVar Miner

List of variants in gene SLC22A5 reported as uncertain significance by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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Total variants: 13
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HGVS dbSNP gnomAD frequency
NM_003060.4(SLC22A5):c.1345T>G (p.Tyr449Asp) rs11568514 0.00114
NM_003060.4(SLC22A5):c.934A>G (p.Ile312Val) rs77300588 0.00085
NM_003060.4(SLC22A5):c.34G>A (p.Gly12Ser) rs139203363 0.00066
NM_003060.4(SLC22A5):c.1451G>T (p.Gly484Val) rs28383480 0.00039
NM_003060.4(SLC22A5):c.287G>C (p.Gly96Ala) rs377767450 0.00029
NM_003060.4(SLC22A5):c.529A>G (p.Met177Val) rs145068530 0.00028
NM_003060.4(SLC22A5):c.761G>A (p.Arg254Gln) rs200699819 0.00007
NM_003060.4(SLC22A5):c.1139C>T (p.Ala380Val) rs746187344 0.00001
NM_003060.4(SLC22A5):c.694A>G (p.Thr232Ala) rs188698686 0.00001
NM_003060.4(SLC22A5):c.932C>G (p.Thr311Ser) rs770408585 0.00001
NM_003060.4(SLC22A5):c.949G>A (p.Glu317Lys) rs774792831 0.00001
NM_003060.4(SLC22A5):c.428C>A (p.Pro143Gln)
NM_003060.4(SLC22A5):c.47C>T (p.Pro16Leu)

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