List of variants in gene IFIH1 reported as uncertain significance for Singleton-Merten syndrome 1

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: 9

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_022168.4(IFIH1):c.2459G>A (p.Arg820His)	rs74162087	0.00025
NM_022168.4(IFIH1):c.1793G>A (p.Arg598His)	rs200945986	0.00011
NM_022168.4(IFIH1):c.527A>G (p.Asn176Ser)	rs374205118	0.00009
NM_022168.4(IFIH1):c.1806A>T (p.Glu602Asp)	rs763549486	0.00001
NM_022168.4(IFIH1):c.1357G>A (p.Val453Met)	rs367921237
NM_022168.4(IFIH1):c.2035_2036del (p.Leu679fs)	rs774076578
NM_022168.4(IFIH1):c.2459G>C (p.Arg820Pro)	rs74162087
NM_022168.4(IFIH1):c.770-10T>C	rs1683038128
NM_022168.4(IFIH1):c.956C>G (p.Ala319Gly)	rs1682931873

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.