List of variants in gene RNF31 reported as pathogenic for immunodeficiency 115 with autoinflammation

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_017999.5(RNF31):c.1197G>C (p.Gln399His)
NM_017999.5(RNF31):c.1737+3A>G	rs2139081076
NM_017999.5(RNF31):c.215T>C (p.Leu72Pro)	rs794729666

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