rs104894361, KRAS

N. diseases: 3
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.
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.882 0.240 12 25245370 missense variant T/A;C;G snv 4.0E-06 0.700 1.000 3 1987 2003
Noonan Syndrome
CUI: C0028326
Disease: Noonan Syndrome
187 0.882 0.240 12 25245370 missense variant T/A;C;G snv 4.0E-06 0.700 1.000 1 2007 2007
CARDIOFACIOCUTANEOUS SYNDROME 2
CUI: C3809005
Disease: CARDIOFACIOCUTANEOUS SYNDROME 2
9 0.882 0.240 12 25245370 missense variant T/A;C;G snv 4.0E-06 0.700 0