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: 6

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HGVS	dbSNP	gnomAD frequency
NM_014989.7(RIMS1):c.1744T>G (p.Ser582Ala)	rs377567871	0.00010
NM_014989.7(RIMS1):c.3002T>C (p.Val1001Ala)	rs770258909	0.00003
NM_014989.7(RIMS1):c.1479G>T (p.Glu493Asp)	rs753784735	0.00001
NM_014989.7(RIMS1):c.3746G>A (p.Arg1249Gln)	rs199933558	0.00001
NM_014989.7(RIMS1):c.1679-20587G>A	rs181193740
NM_014989.7(RIMS1):c.3959C>T (p.Ser1320Phe)	rs140943787

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