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: rs12153855
rs12153855
TNXB
0.776 0.320 6 32107027 intron variant T/C snv 0.11
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.820 1.000 1 2012 2016
dbSNP: rs1150754
rs1150754
TNXB
0.851 0.200 6 32082981 intron variant C/A;T snv
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.810 1.000 1 2011 2017
dbSNP: rs17207986
rs17207986
TNXB
1.000 0.040 6 32111790 non coding transcript exon variant T/C;G snv
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.810 1.000 1 2010 2010
dbSNP: rs12153855
rs12153855
TNXB
0.776 0.320 6 32107027 intron variant T/C snv 0.11
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic 		0.800 1.000 1 2013 2013
dbSNP: rs2857009
rs2857009
TNXB
1.000 0.080 6 32051969 intron variant G/C snv 0.25
CUI: C0577608
Disease: C4 complement assay (procedure)
C4 complement assay (procedure) 		0.800 1.000 1 2012 2012
dbSNP: rs3130342
rs3130342
TNXB
1.000 0.080 6 32112369 non coding transcript exon variant A/C;G;T snv
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.710 1.000 1 2008 2008
dbSNP: rs1150752
rs1150752
TNXB
0.882 0.240 6 32096949 missense variant T/C;G snv 5.9E-02
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 1 2011 2011
dbSNP: rs1150752
rs1150752
TNXB
0.882 0.240 6 32096949 missense variant T/C;G snv 5.9E-02
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		0.700 1.000 1 2009 2009
dbSNP: rs1150752
rs1150752
TNXB
0.882 0.240 6 32096949 missense variant T/C;G snv 5.9E-02
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.700 1.000 1 2007 2007
dbSNP: rs1150753
rs1150753
TNXB
0.925 0.120 6 32092090 intron variant A/G snv 6.3E-02
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 1 2011 2011
dbSNP: rs1150754
rs1150754
TNXB
0.851 0.200 6 32082981 intron variant C/A;T snv
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.700 1.000 1 2007 2007
dbSNP: rs12153855
rs12153855
TNXB
0.776 0.320 6 32107027 intron variant T/C snv 0.11
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.700 1.000 1 2010 2010
dbSNP: rs12153855
rs12153855
TNXB
0.776 0.320 6 32107027 intron variant T/C snv 0.11
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.700 1.000 1 2007 2007
dbSNP: rs12153855
rs12153855
TNXB
0.776 0.320 6 32107027 intron variant T/C snv 0.11
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		0.700 1.000 1 2010 2010
dbSNP: rs12198173
rs12198173
TNXB
0.827 0.240 6 32059031 intron variant G/A snv 0.10
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
Acquired Immunodeficiency Syndrome 		0.700 1.000 1 2009 2009
dbSNP: rs12198173
rs12198173
TNXB
0.827 0.240 6 32059031 intron variant G/A snv 0.10
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.700 1.000 1 2010 2010
dbSNP: rs12198173
rs12198173
TNXB
0.827 0.240 6 32059031 intron variant G/A snv 0.10
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.700 1.000 1 2007 2007
dbSNP: rs12198173
rs12198173
TNXB
0.827 0.240 6 32059031 intron variant G/A snv 0.10
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 1.000 1 2010 2010
dbSNP: rs12198173
rs12198173
TNXB
0.827 0.240 6 32059031 intron variant G/A snv 0.10
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic 		0.700 1.000 1 2013 2013
dbSNP: rs12198173
rs12198173
TNXB
0.827 0.240 6 32059031 intron variant G/A snv 0.10
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.700 1.000 1 2010 2010
dbSNP: rs12198173
rs12198173
TNXB
0.827 0.240 6 32059031 intron variant G/A snv 0.10
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 1.000 1 2010 2010
dbSNP: rs12198173
rs12198173
TNXB
0.827 0.240 6 32059031 intron variant G/A snv 0.10
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.700 1.000 1 2010 2010
dbSNP: rs12211410
rs12211410
TNXB
0.925 0.120 6 32081646 missense variant C/G;T snv 5.6E-05; 7.7E-02; 3.7E-05
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 1.000 1 2010 2010
dbSNP: rs12211410
rs12211410
TNXB
0.925 0.120 6 32081646 missense variant C/G;T snv 5.6E-05; 7.7E-02; 3.7E-05
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic 		0.700 1.000 1 2013 2013
dbSNP: rs12211410
rs12211410
TNXB
0.925 0.120 6 32081646 missense variant C/G;T snv 5.6E-05; 7.7E-02; 3.7E-05
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.700 1.000 1 2010 2010