rs104894359, KRAS

N. diseases: 5
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
NOONAN SYNDROME 3
CUI: C1860991
Disease: NOONAN SYNDROME 3
33 0.851 0.200 12 25227346 missense variant C/G;T snv 0.800 1.000 7 2006 2011
CARDIOFACIOCUTANEOUS SYNDROME 2
CUI: C3809005
Disease: CARDIOFACIOCUTANEOUS SYNDROME 2
9 0.851 0.200 12 25227346 missense variant C/G;T snv 0.800 1.000 5 2006 2012
Cardio-facio-cutaneous syndrome
CUI: C1275081
Disease: Cardio-facio-cutaneous syndrome
82 0.851 0.200 12 25227346 missense variant C/G;T snv 0.700 1.000 3 2006 2011
Noonan Syndrome
CUI: C0028326
Disease: Noonan Syndrome
187 0.851 0.200 12 25227346 missense variant C/G;T snv 0.700 1.000 3 2006 2011
Nodule
CUI: C0028259
Disease: Nodule
19 0.851 0.200 12 25227346 missense variant C/G;T snv 0.010 1.000 1 2001 2001