ClinVar Miner

List of variants in gene SDK1 reported as likely benign 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 7p22.2(chr7:3086310-3703105)x3
GRCh37/hg19 7p22.2-22.1(chr7:3813870-4674445)x3
GRCh38/hg38 7p22.2(chr7:3589872-3697219)x1

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