rs104894230, HRAS;LRRC56

N. diseases: 73
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.
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
235 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2011 2011
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.020 1.000 2 2015 2017
Secondary malignant neoplasm of lymph node
CUI: C0686619
Disease: Secondary malignant neoplasm of lymph node
188 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2015 2015
Transitional cell carcinoma of bladder
CUI: C0279680
Disease: Transitional cell carcinoma of bladder
158 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Malignant Uterine Corpus Neoplasm
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
152 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
leukemia
CUI: C0023418
Disease: leukemia
144 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2014 2014
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
140 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2014 2014
Adenocarcinoma of pancreas
CUI: C0281361
Disease: Adenocarcinoma of pancreas
138 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 5 2007 2016
Cardiac Arrhythmia
CUI: C0003811
Disease: Cardiac Arrhythmia
111 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2006 2006
Adenocarcinoma of prostate
CUI: C0007112
Disease: Adenocarcinoma of prostate
108 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Serous cystadenocarcinoma ovary
CUI: C0279663
Disease: Serous cystadenocarcinoma ovary
99 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
MYELODYSPLASTIC SYNDROME
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
95 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Squamous cell carcinoma of skin
CUI: C0553723
Disease: Squamous cell carcinoma of skin
92 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Uterine Carcinosarcoma
CUI: C0280630
Disease: Uterine Carcinosarcoma
80 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Tumor Progression
CUI: C0178874
Disease: Tumor Progression
72 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2011 2011
Uterine Cervical Neoplasm
CUI: C0007873
Disease: Uterine Cervical Neoplasm
72 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Neuromuscular Diseases
CUI: C0027868
Disease: Neuromuscular Diseases
50 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2017 2017
Chronic myeloproliferative disorder
CUI: C1292778
Disease: Chronic myeloproliferative disorder
47 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2017 2017
Myeloproliferative disease
CUI: C0027022
Disease: Myeloproliferative disease
43 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2017 2017
Nasopharyngeal Neoplasms
CUI: C0027439
Disease: Nasopharyngeal Neoplasms
36 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Arthrogryposis
CUI: C0003886
Disease: Arthrogryposis
33 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2017 2017
Adenoid Cystic Carcinoma
CUI: C0010606
Disease: Adenoid Cystic Carcinoma
30 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Papillary renal cell carcinoma, sporadic
CUI: C1336078
Disease: Papillary renal cell carcinoma, sporadic
30 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016