ClinVar Miner

List of variants in gene RIMS1 reported as uncertain significance by Department of Pathology and Laboratory Medicine,Sinai Health System

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
E493D
NM_001168408.2(RIMS1):c.1741+15320C>T
NM_001350421.2(RIMS1):c.-94G>A

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