ClinVar Miner

List of variants in gene RNF31 reported as likely pathogenic by Institute of Human Genetics, FAU Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg

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_017999.5(RNF31):c.2480G>A (p.Arg827His)	rs377035972	0.00010
NM_017999.5(RNF31):c.2333A>G (p.Tyr778Cys)	rs1566615893

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