List of variants reported as likely pathogenic for Noonan syndrome by 3billion

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: 7

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_002880.4(RAF1):c.709G>A (p.Ala237Thr)	rs587777588	0.00001
NM_002524.5(NRAS):c.449A>G (p.Gln150Arg)	rs2101738598
NM_002834.5(PTPN11):c.184T>A (p.Tyr62Asn)	rs121918460
NM_002834.5(PTPN11):c.663A>G (p.Ile221Met)
NM_005633.4(SOS1):c.805A>G (p.Met269Val)
NM_005633.4(SOS1):c.925G>A (p.Asp309Asn)	rs397517180
NM_012250.6(RRAS2):c.67G>A (p.Gly23Ser)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.