ClinVar Miner

List of variants in gene IFIH1 reported as risk factor for post-COVID-19 disorder

Included ClinVar conditions (4):

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_022168.4(IFIH1):c.1641+1G>C	rs35337543	0.00728
NM_022168.4(IFIH1):c.2016del (p.Asp673fs)	rs773033563	0.00028

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