List of variants in gene NRAS reported as uncertain significance for Noonan 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_002524.4(NRAS):c.-179G>C	rs886045110	0.00002
NM_002524.4(NRAS):c.-209A>G	rs886045111
NM_002524.4(NRAS):c.-242G>C	rs886045112
NM_002524.4(NRAS):c.-245C>T	rs886045113
NM_002524.5(NRAS):c.1062_1063del	rs775070295
NM_002524.5(NRAS):c.*935dup	rs886045106
NM_002524.5(NRAS):c.235C>T (p.Leu79Phe)	rs1659097188
NM_002524.5(NRAS):c.457G>A (p.Glu153Lys)

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