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: rs2252641
rs2252641
TEX41 ; LOC100505498
1.000 0.040 2 145043894 non coding transcript exon variant T/C;G snv 0.58
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.800 1.000 1 2013 2018
dbSNP: rs11681525
rs11681525
TEX41
1.000 0.040 2 144734815 intron variant C/G snv 5.9E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 2 2015 2017
dbSNP: rs11681525
rs11681525
TEX41
1.000 0.040 2 144734815 intron variant C/G snv 5.9E-02
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.700 1.000 2 2015 2017
dbSNP: rs7560871
rs7560871
TEX41
2 144859332 intron variant G/A snv 4.9E-02
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2019 2019
dbSNP: rs1085639
rs1085639
TEX41 ; LOC100505498
2 145152086 non coding transcript exon variant G/A snv 0.61
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs10928224
rs10928224
TEX41
2 144708009 intron variant T/A snv 0.60
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
dbSNP: rs10928235
rs10928235
TEX41
1.000 0.080 2 144920547 intron variant A/T snv 0.18
CUI: C0002170
Disease: Alopecia
Alopecia 		0.700 1.000 1 2017 2017
dbSNP: rs10928235
rs10928235
TEX41
1.000 0.080 2 144920547 intron variant A/T snv 0.18
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs10928240
rs10928240
TEX41 ; LOC100505498
2 145062903 intron variant C/G snv 0.39
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs114964326
rs114964326
TEX41 ; LOC100505498
2 145257661 intron variant G/A snv 1.6E-02
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs115584509
rs115584509
TEX41
2 144872001 intron variant G/A;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs11683692
rs11683692
TEX41
2 144752048 intron variant T/C snv 3.4E-02
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs11691685
rs11691685
TEX41
0.827 0.120 2 144724260 intron variant A/G snv 5.2E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2016 2016
dbSNP: rs11691685
rs11691685
TEX41
0.827 0.120 2 144724260 intron variant A/G snv 5.2E-02
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 1 2016 2016
dbSNP: rs11691685
rs11691685
TEX41
0.827 0.120 2 144724260 intron variant A/G snv 5.2E-02
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2016 2016
dbSNP: rs11691685
rs11691685
TEX41
0.827 0.120 2 144724260 intron variant A/G snv 5.2E-02
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016
dbSNP: rs11691685
rs11691685
TEX41
0.827 0.120 2 144724260 intron variant A/G snv 5.2E-02
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2016 2016
dbSNP: rs1384781
rs1384781
TEX41
2 144843490 intron variant T/C snv 0.60
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs1438896
rs1438896
TEX41
2 144888505 intron variant T/C snv 0.66
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2017 2017
dbSNP: rs1445300
rs1445300
TEX41 ; LOC100505498
1.000 0.040 2 145258379 intron variant A/G snv 8.5E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs17409500
rs17409500
TEX41 ; LOC100505498
1.000 0.040 2 145259004 intron variant A/G snv 0.25
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs1830321
rs1830321
TEX41 ; LOC100505498
0.827 0.080 2 145067988 intron variant C/T snv 0.40
CUI: C0155567
Disease: Rheumatic aortic stenosis
Rheumatic aortic stenosis 		0.700 1.000 1 2018 2018
dbSNP: rs2246363
rs2246363
TEX41 ; LOC100505498
2 145025715 intron variant G/A snv 0.82
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2016 2016
dbSNP: rs2256460
rs2256460
TEX41 ; LOC100505498
2 145035889 intron variant C/T snv 0.32
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs2697329
rs2697329
TEX41 ; LOC100505498
2 145134860 intron variant G/A snv 0.61
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019