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: rs72928038
rs72928038
0.695 0.360 6 90267049 intron variant G/A snv 0.11
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.810 1.000 1 2012 2016
dbSNP: rs11755527
rs11755527
0.851 0.360 6 90248512 intron variant C/G snv 0.36
Diabetes Mellitus, Insulin-Dependent
0.800 1.000 2 2008 2011
dbSNP: rs7753008
rs7753008
1.000 0.080 6 90099920 intron variant T/A;C snv
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
0.800 1.000 2 2011 2012
dbSNP: rs10806425
rs10806425
0.851 0.280 6 90216893 intron variant C/A snv 0.33
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
0.800 1.000 1 2010 2010
dbSNP: rs12212193
rs12212193
0.925 0.280 6 90287050 intron variant A/G snv 0.38
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.800 1.000 1 2011 2011
dbSNP: rs1847472
rs1847472
0.807 0.200 6 90263440 intron variant C/A snv 0.25
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2010 2017
dbSNP: rs1847472
rs1847472
0.807 0.200 6 90263440 intron variant C/A snv 0.25
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 1 2012 2017
dbSNP: rs2474619
rs2474619
0.882 0.360 6 90170316 intron variant C/A snv 0.72
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
0.800 1.000 1 2014 2014
dbSNP: rs3757247
rs3757247
0.827 0.320 6 90247744 intron variant C/T snv 0.38
Diabetes Mellitus, Insulin-Dependent
0.800 1.000 1 2009 2009
dbSNP: rs3757247
rs3757247
0.827 0.320 6 90247744 intron variant C/T snv 0.38
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.800 1.000 1 2012 2012
dbSNP: rs10806425
rs10806425
0.851 0.280 6 90216893 intron variant C/A snv 0.33
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
0.700 1.000 1 2011 2011
dbSNP: rs10806425
rs10806425
0.851 0.280 6 90216893 intron variant C/A snv 0.33
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2011 2011
dbSNP: rs10806425
rs10806425
0.851 0.280 6 90216893 intron variant C/A snv 0.33
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1.000 1 2011 2011
dbSNP: rs10806425
rs10806425
0.851 0.280 6 90216893 intron variant C/A snv 0.33
CUI: C0021053
Disease: Immune System Diseases
Immune System Diseases
0.700 1.000 1 2011 2011
dbSNP: rs11755527
rs11755527
0.851 0.360 6 90248512 intron variant C/G snv 0.36
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1.000 1 2011 2011
dbSNP: rs11755527
rs11755527
0.851 0.360 6 90248512 intron variant C/G snv 0.36
CUI: C1272321
Disease: Autoantibody measurement
Autoantibody measurement
0.700 1.000 1 2011 2011
dbSNP: rs1847472
rs1847472
0.807 0.200 6 90263440 intron variant C/A snv 0.25
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2011 2011
dbSNP: rs4388268
rs4388268
6 90025189 intron variant G/A snv 0.28
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs597325
rs597325
0.925 0.160 6 90292775 intron variant A/G snv 0.69
Diabetes Mellitus, Insulin-Dependent
0.700 1.000 1 2011 2011
dbSNP: rs9444730
rs9444730
6 90023618 intron variant T/C;G snv 0.31
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013