ClinVar Miner

List of intergenic variants reported as benign by GeneReviews

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_001081563.1(DMPK):c.224_226CTG[(5-34)]
SIX3:c.942G>A
TGIF1:c.887C>T

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