List of variants in gene RIPOR2 reported as uncertain significance by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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	gnomAD frequency
NM_001286445.3(RIPOR2):c.1130C>T (p.Pro377Leu)	rs201901775	0.00022
NM_001286445.3(RIPOR2):c.965G>A (p.Arg322Gln)	rs745837159	0.00005
NM_001286445.3(RIPOR2):c.2579T>C (p.Val860Ala)	rs1581507142

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