ClinVar Miner

List of variants in gene NRAS 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_002524.5(NRAS):c.291-8G>A	rs376187980	0.00004
NM_002524.5(NRAS):c.368G>A (p.Arg123Lys)	rs727503347

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