rs104894229, LRRC56;HRAS

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.
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.020 1.000 2 2016 2016
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.020 1.000 2 2012 2020
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.020 1.000 2 2012 2020
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.010 1.000 1 2016 2016
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.564 0.600 11 534289 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 534289 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.700 1.000 9 2005 2009
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.700 1.000 3 2006 2016
Muscle hypotonia
CUI: C0026827
Disease: Muscle hypotonia
579 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.700 1.000 5 2006 2012
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
melanoma
CUI: C0025202
Disease: melanoma
515 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.010 1.000 1 2016 2016
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
385 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Squamous cell carcinoma of the head and neck
CUI: C1168401
Disease: Squamous cell carcinoma of the head and neck
348 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Malignant neoplasm of urinary bladder
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
316 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.700 0
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.700 1.000 1 2014 2014
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.564 0.600 11 534289 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 534289 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 534289 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.010 1.000 1 2017 2017
Noonan Syndrome
CUI: C0028326
Disease: Noonan Syndrome
187 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.010 1.000 1 2007 2007
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.700 1.000 9 2005 2009
Transitional cell carcinoma of bladder
CUI: C0279680
Disease: Transitional cell carcinoma of bladder
158 0.564 0.600 11 534289 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 534289 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016