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: 17

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HGVS	dbSNP	gnomAD frequency
NM_014989.7(RIMS1):c.1083A>G (p.Leu361=)	rs2463730	0.97673
NM_014989.7(RIMS1):c.666A>G (p.Leu222=)	rs2249021	0.68629
NM_014989.7(RIMS1):c.2928-80C>T	rs6923891	0.64993
NM_014989.7(RIMS1):c.1857+61C>T	rs2807519	0.64829
NM_014989.7(RIMS1):c.812+93G>A	rs17725666	0.28367
NM_014989.7(RIMS1):c.1209G>A (p.Ala403=)	rs114505309	0.27986
NM_014989.7(RIMS1):c.4548C>T (p.Phe1516=)	rs2815738	0.20095
NM_014989.7(RIMS1):c.460-37C>T	rs41265489	0.06803
NM_014989.7(RIMS1):c.3482+79A>T	rs6925880	0.05104
NM_014989.7(RIMS1):c.3555-91G>A	rs76570730	0.02947
NM_014989.7(RIMS1):c.3470C>T (p.Pro1157Leu)	rs41265501	0.02135
NM_014989.7(RIMS1):c.3053+74A>T	rs9442761	0.02076
NM_014989.7(RIMS1):c.1679-20565G>A	rs9446600	0.01872
NM_014989.7(RIMS1):c.743C>T (p.Ser248Leu)	rs116476753	0.01648
NM_014989.7(RIMS1):c.3308+84_3308+86del	rs200346289
NM_014989.7(RIMS1):c.4618+20del	rs113359739
NM_014989.7(RIMS1):c.4860+80_4860+81del	rs67994138

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