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: rs6586030
rs6586030
TSPAN14
1.000 0.040 10 80494291 intron variant A/G;T snv
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.800 1.000 2 2012 2017
dbSNP: rs7097656
rs7097656
TSPAN14
0.827 0.120 10 80491075 intron variant T/C;G snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 2 2015 2016
dbSNP: rs10788639
rs10788639
TSPAN14
10 80473469 intron variant C/G snv 0.64
CUI: C0035242
Disease: Respiratory Tract Diseases
Respiratory Tract Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs12220642
rs12220642
TSPAN14
10 80459208 intron variant T/C;G snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs12264252
rs12264252
TSPAN14
1.000 0.040 10 80517585 intron variant G/A snv 0.18
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2018 2018
dbSNP: rs17680741
rs17680741
TSPAN14
1.000 0.040 10 80491758 intron variant T/C snv 0.25
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2018 2018
dbSNP: rs1902661
rs1902661
TSPAN14
1.000 0.040 10 80458350 intron variant G/A;C snv
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		0.700 1.000 1 2019 2019
dbSNP: rs1993484
rs1993484
TSPAN14
10 80462942 intron variant T/C snv 0.82
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2015 2015
dbSNP: rs6586030
rs6586030
TSPAN14
1.000 0.040 10 80494291 intron variant A/G;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2017 2017
dbSNP: rs7086627
rs7086627
TSPAN14
10 80460841 intron variant C/T snv 0.80
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2015 2015
dbSNP: rs7097656
rs7097656
TSPAN14
0.827 0.120 10 80491075 intron variant T/C;G snv
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2016 2016
dbSNP: rs7097656
rs7097656
TSPAN14
0.827 0.120 10 80491075 intron variant T/C;G snv
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2016 2016
dbSNP: rs7097656
rs7097656
TSPAN14
0.827 0.120 10 80491075 intron variant T/C;G snv
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.700 1.000 1 2015 2015
dbSNP: rs7097656
rs7097656
TSPAN14
0.827 0.120 10 80491075 intron variant T/C;G snv
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 1 2016 2016
dbSNP: rs7097656
rs7097656
TSPAN14
0.827 0.120 10 80491075 intron variant T/C;G snv
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016
dbSNP: rs7100689
rs7100689
TSPAN14
10 80462422 intron variant C/A;G snv
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2015 2015