ClinVar Miner

List of variants in gene LINGO2 reported as uncertain significance by ISCA site 1

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
GRCh37/hg19 9p21.1(chr9:28303003-28509732)x1
GRCh37/hg19 9p21.1(chr9:28427025-28725108)x1
GRCh38/hg38 9p21.1(chr9:28030643-28378184)x1

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