ClinVar Miner

List of variants reported as benign for Noonan syndrome 1 by Fulgent Genetics, Fulgent Genetics

Included ClinVar conditions (11):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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_002834.5(PTPN11):c.-273G>A	rs58805176	0.10884
NM_004333.6(BRAF):c.1315-18T>G	rs6959000	0.00840

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