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: 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: rs1150757
rs1150757
TNXB
0.925 0.160 6 32061428 synonymous variant G/A;C snv 5.9E-02
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 1.000 2 2015 2016
dbSNP: rs1150753
rs1150753
TNXB
0.925 0.120 6 32092090 intron variant A/G snv 6.3E-02
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 1.000 1 2016 2016
dbSNP: rs1150754
rs1150754
TNXB
0.851 0.200 6 32082981 intron variant C/A;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2019 2019
dbSNP: rs1150755
rs1150755
TNXB
1.000 0.080 6 32070773 intron variant C/T snv 0.10
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 1.000 1 2017 2017
dbSNP: rs1150757
rs1150757
TNXB
0.925 0.160 6 32061428 synonymous variant G/A;C snv 5.9E-02
CUI: C0027873
Disease: Neuromyelitis Optica
Neuromyelitis Optica 		0.700 1.000 1 2018 2018
dbSNP: rs116298992
rs116298992
TNXB
6 32100718 intron variant C/T snv 1.5E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs13199524
rs13199524
TNXB
0.807 0.240 6 32098988 intron variant C/T snv 8.4E-02
CUI: C0003872
Disease: Arthritis, Psoriatic
Arthritis, Psoriatic 		0.700 1.000 1 2019 2019
dbSNP: rs144433536
rs144433536
TNXB
0.925 0.080 6 32067917 synonymous variant C/A;G;T snv
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung 		0.700 1.000 1 2017 2017
dbSNP: rs144433536
rs144433536
TNXB
0.925 0.080 6 32067917 synonymous variant C/A;G;T snv
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.700 1.000 1 2017 2017
dbSNP: rs185819
rs185819
TNXB
0.851 0.200 6 32082290 missense variant T/A;C;G snv 8.2E-06; 0.58; 4.1E-06
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2008 2008
dbSNP: rs185819
rs185819
TNXB
0.851 0.200 6 32082290 missense variant T/A;C;G snv 8.2E-06; 0.58; 4.1E-06
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2017 2017
dbSNP: rs2021783
rs2021783
TNXB
6 32077074 intron variant C/T snv 1.0E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2015 2015
dbSNP: rs2021783
rs2021783
TNXB
6 32077074 intron variant C/T snv 1.0E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.700 1.000 1 2015 2015
dbSNP: rs2021783
rs2021783
TNXB
6 32077074 intron variant C/T snv 1.0E-02
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2015 2015
dbSNP: rs204883
rs204883
TNXB
1.000 0.120 6 32064966 missense variant G/A;C snv 0.44
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs2856451
rs2856451
TNXB
6 32043581 intron variant A/G;T snv 0.59
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs2856451
rs2856451
TNXB
6 32043581 intron variant A/G;T snv 0.59
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs2856451
rs2856451
TNXB
6 32043581 intron variant A/G;T snv 0.59
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs3130342
rs3130342
TNXB
1.000 0.080 6 32112369 non coding transcript exon variant A/C;G;T snv
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
dbSNP: rs3134954
rs3134954
TNXB
0.882 0.240 6 32104116 intron variant C/T snv 0.90
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018