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: rs10516487
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.880 1.000 2 2008 2019
dbSNP: rs17266594
rs17266594
BANK1
0.807 0.280 4 101829765 intron variant T/C snv 0.25 0.27
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.850 1.000 1 2008 2017
dbSNP: rs13126505
rs13126505
BANK1
1.000 0.040 4 101944147 intron variant G/A snv 4.1E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 2 2012 2017
dbSNP: rs17031508
rs17031508
BANK1
4 101639133 intron variant A/C snv 8.6E-02
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.800 1.000 1 2012 2012
dbSNP: rs17199964
rs17199964
BANK1
4 101786634 intron variant G/A;C snv
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 3 2018 2019
dbSNP: rs13109404
rs13109404
BANK1
4 101975434 intron variant T/G snv 4.1E-02
CUI: C0424574
Disease: Duration of sleep
Duration of sleep 		0.700 1.000 2 2019 2019
dbSNP: rs34592089
rs34592089
BANK1
1.000 0.040 4 102005766 intron variant G/A;T snv
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 2 2018 2019
dbSNP: rs10028805
rs10028805
BANK1
0.882 0.160 4 101816093 intron variant G/A snv 0.45
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 1.000 1 2015 2015
dbSNP: rs10028805
rs10028805
BANK1
0.882 0.160 4 101816093 intron variant G/A snv 0.45
CUI: C0855095
Disease: Small Lymphocytic Lymphoma
Small Lymphocytic Lymphoma 		0.700 1.000 1 2016 2016
dbSNP: rs10028805
rs10028805
BANK1
0.882 0.160 4 101816093 intron variant G/A snv 0.45
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		0.700 1.000 1 2016 2016
dbSNP: rs10516491
rs10516491
BANK1
4 102031709 intron variant T/C snv 6.5E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs13107612
rs13107612
BANK1
0.827 0.120 4 101818823 intron variant C/T snv 0.31
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016
dbSNP: rs13107612
rs13107612
BANK1
0.827 0.120 4 101818823 intron variant C/T snv 0.31
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2016 2016
dbSNP: rs13107612
rs13107612
BANK1
0.827 0.120 4 101818823 intron variant C/T snv 0.31
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2016 2016
dbSNP: rs13107612
rs13107612
BANK1
0.827 0.120 4 101818823 intron variant C/T snv 0.31
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2016 2016
dbSNP: rs13107612
rs13107612
BANK1
0.827 0.120 4 101818823 intron variant C/T snv 0.31
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 1 2016 2016
dbSNP: rs13126505
rs13126505
BANK1
1.000 0.040 4 101944147 intron variant G/A snv 4.1E-02
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs13126505
rs13126505
BANK1
1.000 0.040 4 101944147 intron variant G/A snv 4.1E-02
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.700 1.000 1 2015 2015
dbSNP: rs13127398
rs13127398
BANK1
4 102000547 intron variant T/A snv 4.1E-02
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs17199964
rs17199964
BANK1
4 101786634 intron variant G/A;C snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs17199964
rs17199964
BANK1
4 101786634 intron variant G/A;C snv
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs17199964
rs17199964
BANK1
4 101786634 intron variant G/A;C snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs17199964
rs17199964
BANK1
4 101786634 intron variant G/A;C snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs17248480
rs17248480
BANK1
4 101514108 intron variant G/A snv 1.8E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs17248480
rs17248480
BANK1
4 101514108 intron variant G/A snv 1.8E-02
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2018 2018