List of variants in gene NRAS reported as pathogenic for Large congenital melanocytic nevus

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_002524.5(NRAS):c.181C>A (p.Gln61Lys)	rs121913254
NM_002524.5(NRAS):c.182A>G (p.Gln61Arg)	rs11554290
NM_002524.5(NRAS):c.37G>C (p.Gly13Arg)	rs121434595

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