List of variants in gene RIMS1 reported as uncertain significance for inborn disorder of amino acid metabolism

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_014989.7(RIMS1):c.2758G>A (p.Val920Ile)	rs376566413	0.00004
NM_014989.7(RIMS1):c.3338G>C (p.Arg1113Thr)	rs2154175134

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