List of variants in gene NRAS reported as benign for RASopathy

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_002524.5(NRAS):c.225C>T (p.Gly75=)	rs142739534	0.00123
NM_002524.5(NRAS):c.36T>G (p.Gly12=)	rs759764705	0.00006
NM_002524.5(NRAS):c.159G>A (p.Leu53=)	rs114668710	0.00001
NM_002524.5(NRAS):c.112-24dup	rs780595451
NM_002524.5(NRAS):c.222A>G (p.Thr74=)
NM_002524.5(NRAS):c.451-11dup
NM_002524.5(NRAS):c.451-19dup
NM_002524.5(NRAS):c.451-21_451-19del	rs754048062

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