ClinVar Miner

List of variants in gene ROR2 reported as benign for autosomal dominant Robinow syndrome

Included ClinVar conditions (4):

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_004560.4(ROR2):c.2455G>A (p.Val819Ile)	rs10761129	0.71630
NM_004560.4(ROR2):c.*170AG[1]	rs140581955

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