ClinVar Miner

List of variants in gene RAET1L reported as benign by Labcorp Genetics (formerly Invitae), 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_130900.3(RAET1L):c.362T>C (p.Leu121Pro)	rs9479413	0.03046
NM_130900.3(RAET1L):c.369A>C (p.Ala123=)	rs201609351	0.01575

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