List of variants in gene IFIH1 reported as likely pathogenic by CeGaT Center for Human Genetics Tuebingen

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_022168.4(IFIH1):c.2016del (p.Asp673fs)	rs773033563	0.00028
NM_022168.4(IFIH1):c.2045-1G>A	rs748813106	0.00003
NM_022168.4(IFIH1):c.505A>T (p.Lys169Ter)	rs201495678	0.00001
NM_022168.4(IFIH1):c.1165G>A (p.Gly389Arg)	rs1576227162

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