List of variants in gene RFX6 reported as likely benign for diabetes mellitus

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_173560.4(RFX6):c.2176C>G (p.Arg726Gly)	rs144648002	0.00436
NM_173560.4(RFX6):c.2399G>C (p.Gly800Ala)	rs138343620	0.00225
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.268G>A (p.Ala90Thr)	rs377721888	0.00049
NM_173560.4(RFX6):c.1930C>T (p.Pro644Ser)	rs762488509
NM_173560.4(RFX6):c.1955G>A (p.Arg652Gln)	rs867520268

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