ClinVar Miner

List of variants in gene combination MIR140, WWP2 reported as pathogenic by Rare Disease Group, Clinical Genetics, Karolinska Institutet

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: 1

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HGVS	dbSNP	gnomAD frequency
NM_001270454.2(WWP2):c.1683-866A>G	rs1567443039

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