Source: GWASDB

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: 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 4 2007 2016
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 3 2007 2018
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: 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: 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: rs498422
rs498422
TSBP1 ; TSBP1-AS1
0.882 0.160 6 32318984 intron variant T/G snv 0.14
CUI: C4021107
Disease: Non-obstructive azoospermia
Non-obstructive azoospermia 		0.710 1.000 1 2012 2017
dbSNP: rs9268368
rs9268368
TSBP1 ; TSBP1-AS1
1.000 0.120 6 32366178 missense variant T/C snv 0.42 0.33
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 4 2007 2011
dbSNP: rs9268384
rs9268384
TSBP1 ; TSBP1-AS1
1.000 0.120 6 32368809 missense variant A/G snv 0.41 0.33
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 4 2007 2011
dbSNP: rs1003878
rs1003878
TSBP1 ; TSBP1-AS1
0.882 0.200 6 32332045 stop gained G/A snv 0.19 0.23
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 3 2007 2011
dbSNP: rs1033500
rs1033500
TSBP1 ; TSBP1-AS1
1.000 0.120 6 32339605 missense variant G/A snv 0.40 0.33
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 3 2007 2011
dbSNP: rs2076537
rs2076537
TSBP1 ; TSBP1-AS1
0.925 0.200 6 32349858 non coding transcript exon variant G/A snv 0.37 0.42
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 3 2007 2011
dbSNP: rs3129939
rs3129939
TSBP1 ; TSBP1-AS1
0.827 0.360 6 32368989 intron variant A/G snv 0.14
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 3 2007 2011
dbSNP: rs3129941
rs3129941
TSBP1 ; TSBP1-AS1
0.882 0.240 6 32369909 missense variant A/G;T snv 0.81
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 3 2007 2011
dbSNP: rs3129943
rs3129943
TSBP1 ; TSBP1-AS1
0.851 0.240 6 32370918 intron variant A/G snv 0.26
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 3 2007 2011
dbSNP: rs547077
rs547077
TSBP1 ; TSBP1-AS1
1.000 0.120 6 32321541 intron variant T/C snv 0.34
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 3 2007 2011
dbSNP: rs6457536
rs6457536
TSBP1 ; TSBP1-AS1
0.882 0.200 6 32305988 intron variant A/G snv 0.21
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 3 2007 2011
dbSNP: rs6935269
rs6935269
TSBP1 ; TSBP1-AS1
0.925 0.120 6 32292573 intron variant T/C snv 0.25
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 3 2007 2011
dbSNP: rs7775397
rs7775397
TSBP1 ; TSBP1-AS1
0.790 0.400 6 32293475 missense variant T/G snv 6.0E-02 6.4E-02
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 3 2007 2011
dbSNP: rs9405090
rs9405090
TSBP1 ; TSBP1-AS1
1.000 0.120 6 32330595 missense variant A/G snv 0.42 0.33
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 3 2007 2009