Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs909253
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.020 1.000 2 2015 2018
dbSNP: rs909253
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.020 1.000 2 2012 2018
dbSNP: rs909253
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.020 1.000 2 2012 2018
dbSNP: rs909253
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.020 0.500 2 2006 2019
dbSNP: rs909253
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.020 1.000 2 2015 2019
dbSNP: rs909253
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.020 0.500 2 2006 2013
dbSNP: rs909253
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv
CUI: C0376545
Disease: Hematologic Neoplasms
Hematologic Neoplasms 		0.010 1.000 1 2014 2014
dbSNP: rs909253
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.010 1.000 1 2015 2015
dbSNP: rs909253
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv
CUI: C1302547
Disease: Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma 		0.010 1.000 1 2015 2015
dbSNP: rs909253
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv
CUI: C0006271
Disease: Bronchiolitis
Bronchiolitis 		0.010 1.000 1 2009 2009
dbSNP: rs909253
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv
CUI: C0278704
Disease: Malignant Childhood Neoplasm
Malignant Childhood Neoplasm 		0.010 1.000 1 2013 2013
dbSNP: rs909253
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.010 1.000 1 2014 2014
dbSNP: rs909253
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv
CUI: C0006277
Disease: Bronchitis
Bronchitis 		0.010 1.000 1 2017 2017
dbSNP: rs909253
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv
CUI: C0338480
Disease: Common Migraine
Common Migraine 		0.010 1.000 1 2014 2014
dbSNP: rs909253
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.010 1.000 1 2014 2014
dbSNP: rs909253
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv
CUI: C0001418
Disease: Adenocarcinoma
Adenocarcinoma 		0.010 1.000 1 2014 2014
dbSNP: rs909253
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv
CUI: C0375023
Disease: Respiratory syncytial virus (RSV) infection in conditions classified elsewhere and of unspecified site
Respiratory syncytial virus (RSV) infection in conditions classified elsewhere and of unspecified site 		0.010 1.000 1 2009 2009
dbSNP: rs909253
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv
CUI: C0004096
Disease: Asthma
Asthma 		0.010 1.000 1 2012 2012
dbSNP: rs909253
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.010 1.000 1 2017 2017
dbSNP: rs909253
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv
CUI: C0243026
Disease: Sepsis
Sepsis 		0.010 1.000 1 2016 2016
dbSNP: rs909253
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
Lymphoma, Non-Hodgkin 		0.010 1.000 1 2009 2009
dbSNP: rs909253
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv
CUI: C0036690
Disease: Septicemia
Septicemia 		0.010 1.000 1 2016 2016
dbSNP: rs909253
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv
CUI: C0154723
Disease: Migraine with Aura
Migraine with Aura 		0.010 1.000 1 2014 2014
dbSNP: rs909253
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.010 1.000 1 2015 2015
dbSNP: rs909253
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv
CUI: C1847835
Disease: VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding) 		0.010 1.000 1 2013 2013