ClinVar Miner

List of variants in gene RTN2 reported as likely pathogenic by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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_005619.5(RTN2):c.938dup (p.Thr314fs)	rs748397131
NM_206900.3(RTN2):c.814+791_814+801del	rs1568624823

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