ClinVar Miner

List of variants in gene EFL1 reported as uncertain significance by Undiagnosed Diseases Network, NIH

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_024580.6(EFL1):c.1232T>A (p.Ile411Asn)	rs775430621	0.00001
NM_024580.6(EFL1):c.1971C>G (p.His657Gln)	rs779232326

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