List of variants in gene RFX6 studied for Monogenic diabetes

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 12

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
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.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.2561C>T (p.Ser854Leu)	rs201522681	0.00093
NM_173560.4(RFX6):c.268G>A (p.Ala90Thr)	rs377721888	0.00049
NM_173560.4(RFX6):c.2412C>G (p.Ser804Arg)	rs751261241	0.00003
NM_173560.4(RFX6):c.1319A>G (p.Tyr440Cys)	rs1018054636
NM_173560.4(RFX6):c.1930C>T (p.Pro644Ser)	rs762488509
NM_173560.4(RFX6):c.1955G>A (p.Arg652Gln)	rs867520268
NM_173560.4(RFX6):c.878A>C (p.His293Pro)	rs1775460105

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.