ClinVar Miner

List of variants in gene RFX6 reported by Genetic Services Laboratory, University of Chicago

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Gene type:
ClinVar version:
Total variants: 17
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HGVS dbSNP gnomAD frequency
NM_173560.4(RFX6):c.1914T>C (p.Gly638=) rs611349 0.23550
NM_173560.4(RFX6):c.1542T>C (p.Asn514=) rs7770158 0.23461
NM_173560.4(RFX6):c.1383T>C (p.Thr461=) rs7764347 0.23095
NM_173560.4(RFX6):c.1328-10T>C rs182606018 0.01645
NM_173560.4(RFX6):c.2166C>T (p.Thr722=) rs73765886 0.01325
NM_173560.4(RFX6):c.1327C>T (p.His443Tyr) rs77146142 0.01320
NM_173560.4(RFX6):c.2176C>G (p.Arg726Gly) rs144648002 0.00436
NM_173560.4(RFX6):c.985G>A (p.Val329Ile) rs139343836 0.00291
NM_173560.4(RFX6):c.2369G>A (p.Gly790Glu) rs57924353 0.00124
NM_173560.4(RFX6):c.2039C>A (p.Thr680Lys) rs146081967 0.00111
NM_173560.4(RFX6):c.2553G>T (p.Gln851His) rs145117989 0.00070
NM_173560.4(RFX6):c.1927C>T (p.Pro643Ser) rs572059852 0.00064
NM_173560.4(RFX6):c.2438G>C (p.Arg813Thr) rs142162854 0.00061
NM_173560.4(RFX6):c.2078A>G (p.Asn693Ser)
NM_173560.4(RFX6):c.2247T>C (p.Tyr749=)
NM_173560.4(RFX6):c.541C>T (p.Arg181Trp) rs587780440
NM_173560.4(RFX6):c.644G>A (p.Arg215Lys) rs2114672832

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