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.
Precancerous Conditions
CUI: C0032927
Disease: Precancerous Conditions
18 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2015 2015
Seborrheic keratosis
CUI: C0022603
Disease: Seborrheic keratosis
21 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2014 2014
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
Thymic Carcinoma
CUI: C0205969
Disease: Thymic Carcinoma
8 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2009 2009
Thymoma
CUI: C0040100
Disease: Thymoma
20 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.010 1.000 1 2009 2009
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
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
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.020 1.000 2 2006 2015
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.020 1.000 2 2006 2015
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.040 1.000 4 2011 2015
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.100 1.000 13 2010 2019
Multiple congenital anomalies
CUI: C0000772
Disease: Multiple congenital anomalies
350 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 10 2002 2017
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
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
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
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
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
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
248 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
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
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 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
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 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