List of variants in gene RTN2 reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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_005619.5(RTN2):c.110T>G (p.Leu37Arg)	rs369180811	0.00005
NM_005619.5(RTN2):c.943C>T (p.Pro315Ser)	rs765944441	0.00001
NM_005619.5(RTN2):c.1185G>C (p.Arg395Ser)	rs781104615
NM_005619.5(RTN2):c.1217G>A (p.Arg406Gln)	rs369158895
NM_005619.5(RTN2):c.1451-1G>A
NM_005619.5(RTN2):c.233G>T (p.Arg78Leu)	rs143302045

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