CCL5, C-C motif chemokine ligand 5, 6352

N. diseases: 514; N. variants: 6
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: rs2107538
rs2107538
0.763 0.360 17 35880776 5 prime UTR variant C/T snv 0.27
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs2107538
rs2107538
0.763 0.360 17 35880776 5 prime UTR variant C/T snv 0.27
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
Infections 0.020 1.000 2 2011 2013
dbSNP: rs2280788
rs2280788
0.925 0.040 17 35880401 5 prime UTR variant G/C snv 2.0E-02
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
Infections 0.020 1.000 2 2011 2013
dbSNP: rs2107538
rs2107538
0.763 0.360 17 35880776 5 prime UTR variant C/T snv 0.27
Diabetes Mellitus, Insulin-Dependent
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2006 2006
dbSNP: rs2107538
rs2107538
0.763 0.360 17 35880776 5 prime UTR variant C/T snv 0.27
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
Benign Prostatic Hyperplasia
Male Urogenital Diseases 0.010 1.000 1 2019 2019
dbSNP: rs2107538
rs2107538
0.763 0.360 17 35880776 5 prime UTR variant C/T snv 0.27
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2014 2014
dbSNP: rs2107538
rs2107538
0.763 0.360 17 35880776 5 prime UTR variant C/T snv 0.27
CUI: C0035204
Disease: Respiration Disorders
Respiration Disorders
Respiratory Tract Diseases 0.010 1.000 1 2015 2015
dbSNP: rs2107538
rs2107538
0.763 0.360 17 35880776 5 prime UTR variant C/T snv 0.27
CUI: C0151332
Disease: Active tuberculosis
Active tuberculosis
Infections 0.010 1.000 1 2011 2011
dbSNP: rs2107538
rs2107538
0.763 0.360 17 35880776 5 prime UTR variant C/T snv 0.27
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma
Neoplasms; Endocrine System Diseases 0.010 < 0.001 1 2013 2013
dbSNP: rs2107538
rs2107538
0.763 0.360 17 35880776 5 prime UTR variant C/T snv 0.27
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs2107538
rs2107538
0.763 0.360 17 35880776 5 prime UTR variant C/T snv 0.27
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2014 2014
dbSNP: rs2107538
rs2107538
0.763 0.360 17 35880776 5 prime UTR variant C/T snv 0.27
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2013 2013
dbSNP: rs2280788
rs2280788
0.925 0.040 17 35880401 5 prime UTR variant G/C snv 2.0E-02
CUI: C0151332
Disease: Active tuberculosis
Active tuberculosis
Infections 0.010 1.000 1 2011 2011
dbSNP: rs2280789
rs2280789
0.925 0.080 17 35879999 intron variant A/G snv 0.16
CUI: C0035204
Disease: Respiration Disorders
Respiration Disorders
Respiratory Tract Diseases 0.010 1.000 1 2015 2015
dbSNP: rs2280789
rs2280789
0.925 0.080 17 35879999 intron variant A/G snv 0.16
CUI: C0041327
Disease: Tuberculosis, Pulmonary
Tuberculosis, Pulmonary
Infections; Respiratory Tract Diseases 0.010 1.000 1 2018 2018
dbSNP: rs2280789
rs2280789
0.925 0.080 17 35879999 intron variant A/G snv 0.16
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
Infections 0.010 1.000 1 2018 2018
dbSNP: rs3817655
rs3817655
1.000 0.080 17 35872637 intron variant A/T snv 0.27
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
Digestive System Diseases; Infections 0.010 1.000 1 2019 2019
dbSNP: rs3817656
rs3817656
1.000 0.080 17 35872158 3 prime UTR variant A/C;G snv
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
Digestive System Diseases; Infections 0.010 1.000 1 2018 2018
dbSNP: rs766662990
rs766662990
0.851 0.120 17 35878529 missense variant C/T snv 1.6E-05 7.0E-06
CUI: C2363741
Disease: HIV-1 infection
HIV-1 infection
0.010 1.000 1 2006 2006
dbSNP: rs766662990
rs766662990
0.851 0.120 17 35878529 missense variant C/T snv 1.6E-05 7.0E-06
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.010 1.000 1 2004 2004
dbSNP: rs766662990
rs766662990
0.851 0.120 17 35878529 missense variant C/T snv 1.6E-05 7.0E-06
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
Alzheimer Disease, Late Onset
Nervous System Diseases; Mental Disorders 0.010 1.000 1 2004 2004
dbSNP: rs766662990
rs766662990
0.851 0.120 17 35878529 missense variant C/T snv 1.6E-05 7.0E-06
CUI: C0003165
Disease: Anthracosis
Anthracosis
Respiratory Tract Diseases 0.010 1.000 1 2006 2006