ClinVar Miner

List of variants in gene CELF2 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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_001326317.2(CELF2):c.-49G>A
NM_001326317.2(CELF2):c.-55-73833G>A
NM_001326342.2(CELF2):c.923A>G (p.Asn308Ser)

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