Variant: rs267606920 

    present in Gene: NRAS
    present in Chromosome: 1
    Position on Chromosome: 114713911
    Alleles of this Variant: C/T

rs267606920 in NRAS gene and Noonan Syndrome 6 PMID 19966803 2010 A restricted spectrum of NRAS mutations causes Noonan syndrome.

PMID 20876176 2010 Noonan syndrome: clinical features, diagnosis, and management guidelines.