ClinVar Miner

List of variants in gene RIMS1 reported as benign for Cone-Rod Dystrophy, Dominant

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_014989.7(RIMS1):c.*1453dup	rs537509888
NM_014989.7(RIMS1):c.4618+20del	rs113359739

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