rs104894365, KRAS

N. diseases: 9
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 0.827 0.320 12 25245345 missense variant C/T snv 0.800 1.000 11 2006 2014
Noonan Syndrome
CUI: C0028326
Disease: Noonan Syndrome
187 0.827 0.320 12 25245345 missense variant C/T snv 0.720 1.000 9 2006 2018
Cardio-facio-cutaneous syndrome
CUI: C1275081
Disease: Cardio-facio-cutaneous syndrome
82 0.827 0.320 12 25245345 missense variant C/T snv 0.700 1.000 6 2006 2011
Chronic myeloproliferative disorder
CUI: C1292778
Disease: Chronic myeloproliferative disorder
47 0.827 0.320 12 25245345 missense variant C/T snv 0.010 1.000 1 2016 2016
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.827 0.320 12 25245345 missense variant C/T snv 0.010 1.000 1 2016 2016
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.827 0.320 12 25245345 missense variant C/T snv 0.010 1.000 1 2016 2016
Pancreatitis
CUI: C0030305
Disease: Pancreatitis
80 0.827 0.320 12 25245345 missense variant C/T snv 0.010 1.000 1 2016 2016
Primary Lesion
CUI: C1402294
Disease: Primary Lesion
8 0.827 0.320 12 25245345 missense variant C/T snv 0.010 1.000 1 2019 2019
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.827 0.320 12 25245345 missense variant C/T snv 0.010 1.000 1 2016 2016