List of variants in gene RIMS1 reported as benign by GeneDx

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: 6

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HGVS	dbSNP
NM_014989.5(RIMS1):c.1083A>G (p.Leu361=)	rs2463730
NM_014989.5(RIMS1):c.1209G>A (p.Ala403=)	rs114505309
NM_014989.5(RIMS1):c.1857+61C>T	rs2807519
NM_014989.5(RIMS1):c.2928-80C>T	rs6923891
NM_014989.5(RIMS1):c.4548C>T (p.Phe1516=)	rs2815738
NM_014989.5(RIMS1):c.666A>G (p.Leu222=)	rs2249021

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