LOC284454, uncharacterized LOC284454, 284454

N. diseases: 6; N. variants: 7
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs895819
rs895819
0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38
Malignant neoplasm of colon and/or rectum
0.060 0.833 6 2012 2020
dbSNP: rs10422126
rs10422126
19 13837498 non coding transcript exon variant G/A snv 0.37
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2016 2016
dbSNP: rs10422126
rs10422126
19 13837498 non coding transcript exon variant G/A snv 0.37
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs11671784
rs11671784
0.790 0.240 19 13836482 non coding transcript exon variant G/A snv 1.2E-02 1.2E-02
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.010 1.000 1 2014 2014
dbSNP: rs62122064
rs62122064
19 13839392 non coding transcript exon variant A/G;T snv
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 1 2019 2019
dbSNP: rs8101375
rs8101375
19 13837583 non coding transcript exon variant T/C;G snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019
dbSNP: rs895819
rs895819
0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38
Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site
0.010 1.000 1 2017 2017
dbSNP: rs895819
rs895819
0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.010 1.000 1 2014 2014
dbSNP: rs895819
rs895819
0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38
CUI: C0334037
Disease: Intestinal metaplasia
Intestinal metaplasia
0.010 < 0.001 1 2013 2013
dbSNP: rs895819
rs895819
0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2012 2012
dbSNP: rs895819
rs895819
0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.010 1.000 1 2019 2019
dbSNP: rs895819
rs895819
0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs895819
rs895819
0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38
CUI: C0017154
Disease: Gastritis, Atrophic
Gastritis, Atrophic
Digestive System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs895819
rs895819
0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.100 0.900 10 2012 2020
dbSNP: rs895819
rs895819
0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
Digestive System Diseases; Neoplasms 0.060 0.833 6 2010 2019
dbSNP: rs895819
rs895819
0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
Digestive System Diseases; Neoplasms 0.060 0.833 6 2010 2019
dbSNP: rs11671784
rs11671784
0.790 0.240 19 13836482 non coding transcript exon variant G/A snv 1.2E-02 1.2E-02
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
Digestive System Diseases; Neoplasms 0.020 1.000 2 2014 2014
dbSNP: rs11671784
rs11671784
0.790 0.240 19 13836482 non coding transcript exon variant G/A snv 1.2E-02 1.2E-02
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
Digestive System Diseases; Neoplasms 0.020 1.000 2 2014 2014
dbSNP: rs895819
rs895819
0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms
Digestive System Diseases; Neoplasms 0.020 0.500 2 2019 2020
dbSNP: rs895819
rs895819
0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma
Digestive System Diseases; Neoplasms 0.010 < 0.001 1 2017 2017
dbSNP: rs895819
rs895819
0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus
Digestive System Diseases; Neoplasms 0.010 < 0.001 1 2017 2017
dbSNP: rs895819
rs895819
0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
Digestive System Diseases; Neoplasms 0.010 < 0.001 1 2017 2017
dbSNP: rs895819
rs895819
0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38
CUI: C0011847
Disease: Diabetes
Diabetes
Endocrine System Diseases 0.020 0.500 2 2016 2019
dbSNP: rs11671784
rs11671784
0.790 0.240 19 13836482 non coding transcript exon variant G/A snv 1.2E-02 1.2E-02
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
Eye Diseases 0.010 1.000 1 2019 2019
dbSNP: rs895819
rs895819
0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38
CUI: C0019693
Disease: HIV Infections
HIV Infections
Infections; Immune System Diseases 0.010 < 0.001 1 2016 2016