ClinVar Miner

List of variants in gene ERF reported as uncertain significance by Klinisk genetik och genomik Research, Gothenburg University

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_006494.4(ERF):c.1300G>A (p.Glu434Lys)	rs749808726	0.00001
NM_006494.4(ERF):c.383T>G (p.Val128Gly)	rs781452659

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