Source: GWASCAT

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: rs2076530
rs2076530
BTNL2 ; TSBP1-AS1
0.724 0.640 6 32396039 missense variant T/C snv 0.42 0.40
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis 		0.900 0.933 1 2005 2019
dbSNP: rs3129934
rs3129934
TSBP1 ; TSBP1-AS1
0.925 0.160 6 32368410 intron variant T/C snv 0.83
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.810 1.000 2 2007 2018
dbSNP: rs3817963
rs3817963
BTNL2 ; TSBP1-AS1
0.776 0.360 6 32400310 intron variant T/C snv 0.25
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		0.810 1.000 2 2012 2017
dbSNP: rs10947262
rs10947262
BTNL2 ; TSBP1-AS1
0.925 0.040 6 32405535 non coding transcript exon variant C/T snv 0.12
CUI: C0409959
Disease: Osteoarthritis, Knee
Osteoarthritis, Knee 		0.810 1.000 1 2010 2010
dbSNP: rs3117098
rs3117098
HCG23 ; TSBP1-AS1
0.851 0.280 6 32390736 non coding transcript exon variant G/A snv 0.72
CUI: C0004096
Disease: Asthma
Asthma 		0.810 1.000 1 2011 2020
dbSNP: rs6910071
rs6910071
TSBP1 ; TSBP1-AS1
0.790 0.320 6 32315077 intron variant A/G snv 0.14
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.810 1.000 1 2007 2016
dbSNP: rs7758128
rs7758128
TSBP1-AS1
0.882 0.040 6 32377506 intron variant C/A;T snv 4.2E-02
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.810 1.000 1 2011 2011
dbSNP: rs10947261
rs10947261
BTNL2 ; TSBP1-AS1
0.882 0.240 6 32405455 splice region variant G/T snv 0.11
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2014 2014
dbSNP: rs1980493
rs1980493
BTNL2 ; TSBP1-AS1
0.776 0.400 6 32395438 intron variant T/C snv 0.13
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.800 1.000 1 2007 2015
dbSNP: rs2050190
rs2050190
TSBP1 ; TSBP1-AS1
1.000 0.120 6 32371299 intron variant A/G snv 0.35
CUI: C0030605
Disease: Activated Partial Thromboplastin Time measurement
Activated Partial Thromboplastin Time measurement 		0.800 1.000 1 2012 2012
dbSNP: rs2076529
rs2076529
BTNL2 ; TSBP1-AS1
1.000 0.120 6 32396178 synonymous variant T/C snv 0.41 0.39
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.800 1.000 1 2010 2010
dbSNP: rs2273017
rs2273017
TSBP1 ; TSBP1-AS1
1.000 0.120 6 32369853 intron variant G/A;C snv 0.59
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.800 1.000 1 2011 2011
dbSNP: rs2395148
rs2395148
TSBP1 ; TSBP1-AS1
0.882 0.200 6 32353777 intron variant G/T snv 4.6E-02
CUI: C3495559
Disease: Juvenile arthritis
Juvenile arthritis 		0.800 1.000 1 2008 2008
dbSNP: rs2395148
rs2395148
TSBP1 ; TSBP1-AS1
0.882 0.200 6 32353777 intron variant G/T snv 4.6E-02
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.800 1.000 1 2009 2009
dbSNP: rs3129900
rs3129900
TSBP1 ; TSBP1-AS1
0.882 0.200 6 32338202 intron variant G/T snv 0.83
CUI: C4277682
Disease: Chemical and Drug Induced Liver Injury
Chemical and Drug Induced Liver Injury 		0.800 1.000 1 2010 2010
dbSNP: rs3129943
rs3129943
TSBP1 ; TSBP1-AS1
0.851 0.240 6 32370918 intron variant A/G snv 0.26
CUI: C0004096
Disease: Asthma
Asthma 		0.800 1.000 1 2011 2011
dbSNP: rs3130340
rs3130340
TSBP1-AS1
0.851 0.200 6 32276850 intron variant T/C snv 0.25
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2008 2008
dbSNP: rs3763309
rs3763309
BTNL2 ; TSBP1-AS1
0.882 0.160 6 32408196 upstream gene variant C/A;T snv
CUI: C0004096
Disease: Asthma
Asthma 		0.800 1.000 1 2011 2018
dbSNP: rs3763309
rs3763309
BTNL2 ; TSBP1-AS1
0.882 0.160 6 32408196 upstream gene variant C/A;T snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.800 1.000 1 2007 2014
dbSNP: rs3806156
rs3806156
BTNL2 ; TSBP1-AS1
0.827 0.280 6 32405921 intron variant G/A;T snv
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.800 1.000 1 2010 2012
dbSNP: rs3817963
rs3817963
BTNL2 ; TSBP1-AS1
0.776 0.360 6 32400310 intron variant T/C snv 0.25
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.800 1.000 1 2013 2013
dbSNP: rs926070
rs926070
TSBP1 ; TSBP1-AS1
0.827 0.320 6 32289789 intron variant G/A snv 0.68
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		0.800 1.000 1 2014 2014
dbSNP: rs9268402
rs9268402
TSBP1 ; TSBP1-AS1
0.827 0.200 6 32373576 intron variant G/A snv 0.45
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.800 1.000 1 2012 2012
dbSNP: rs9469099
rs9469099
TSBP1 ; TSBP1-AS1
1.000 0.120 6 32341131 intron variant G/A;T snv
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic 		0.800 1.000 1 2012 2012
dbSNP: rs13196329
rs13196329
TSBP1 ; TSBP1-AS1
0.925 0.120 6 32357594 intron variant A/C snv 2.6E-02
CUI: C0152266
Disease: Mixed Cellularity Hodgkin Lymphoma
Mixed Cellularity Hodgkin Lymphoma 		0.710 1.000 1 2017 2017