List of variants in gene combination LOC129931249, 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_002524.5(NRAS):c.-106G>T	rs755583487	0.00020
NM_002524.4(NRAS):c.-132C>T	rs886045109

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