List of variants in gene NRAS reported as likely benign for Noonan syndrome and Noonan-related syndrome

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: 21

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HGVS	dbSNP	gnomAD frequency
NM_002524.4(NRAS):c.-208T>A	rs2273267	0.01703
NM_002524.5(NRAS):c.*416A>C	rs9724643	0.01360
NM_002524.5(NRAS):c.*3499C>T	rs147926293	0.00568
NM_002524.5(NRAS):c.*3366G>T	rs72994440	0.00380
NM_002524.5(NRAS):c.*3219C>G	rs72994441	0.00379
NM_002524.5(NRAS):c.*2517A>G	rs554048037	0.00142
NM_002524.5(NRAS):c.*3306A>G	rs189738278	0.00124
NM_002524.5(NRAS):c.225C>T (p.Gly75=)	rs142739534	0.00109
NM_002524.5(NRAS):c.*2464A>G	rs140878667	0.00041
NM_002524.5(NRAS):c.360G>A (p.Leu120=)	rs143020946	0.00034
NM_002524.5(NRAS):c.112-8A>G	rs9724626	0.00024
NM_002524.5(NRAS):c.*2784T>A	rs374889066	0.00021
NM_002524.5(NRAS):c.*583T>G	rs555171083	0.00021
NM_002524.5(NRAS):c.*2816T>C	rs370262800	0.00011
NM_002524.5(NRAS):c.*2327C>T	rs533027827	0.00008
NM_002524.5(NRAS):c.*3500G>A	rs528970050	0.00005
NM_002524.5(NRAS):c.36T>G (p.Gly12=)	rs759764705	0.00005
NM_002524.5(NRAS):c.553C>T (p.Pro185Ser)	rs374061873	0.00003
NM_002524.5(NRAS):c.2510_2515del	rs549171175
NM_002524.5(NRAS):c.*2965del	rs61652108
NM_002524.5(NRAS):c.443C>T (p.Thr148Ile)	rs2101738617

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