ClinVar Miner

List of variants in gene ANLN reported as uncertain significance by Gharavi Laboratory, Columbia 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_018685.5(ANLN):c.2454_2465del (p.Cys819_Val822del)	rs1562804930
NM_018685.5(ANLN):c.2476+2T>A	rs1562805029

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