List of variants in gene RTN2 reported as uncertain significance 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_005619.5(RTN2):c.939del (p.Thr314fs)	rs768449676	0.00006
NM_005619.4(RTN2):c.818_828del	rs1568624823
NM_005619.5(RTN2):c.1258G>A (p.Asp420Asn)
NM_005619.5(RTN2):c.1384G>T (p.Ala462Ser)
NM_005619.5(RTN2):c.198C>A (p.Tyr66Ter)	rs2513743882
NM_005619.5(RTN2):c.472del (p.Glu158fs)	rs2122227622
NM_005619.5(RTN2):c.646G>T (p.Ala216Ser)	rs748249548
NM_005619.5(RTN2):c.714G>C (p.Glu238Asp)	rs2513741942
NM_005619.5(RTN2):c.71C>A (p.Ser24Tyr)
NM_005619.5(RTN2):c.934C>G (p.Pro312Ala)	rs2122224100

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