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: rs2395182
rs2395182
0.851 0.280 6 32445540 downstream gene variant G/T snv 0.76
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 3 2007 2011
dbSNP: rs2395182
rs2395182
0.851 0.280 6 32445540 downstream gene variant G/T snv 0.76
Diabetes Mellitus, Insulin-Dependent
0.700 1.000 1 2007 2007
dbSNP: rs2395182
rs2395182
0.851 0.280 6 32445540 downstream gene variant G/T snv 0.76
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1.000 1 2010 2010
dbSNP: rs2395182
rs2395182
0.851 0.280 6 32445540 downstream gene variant G/T snv 0.76
CUI: C0149678
Disease: Epstein-Barr Virus Infections
Epstein-Barr Virus Infections
0.700 1.000 1 2013 2013
dbSNP: rs2395182
rs2395182
0.851 0.280 6 32445540 downstream gene variant G/T snv 0.76
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
0.700 1.000 1 2012 2012
dbSNP: rs3129869
rs3129869
1.000 0.120 6 32437894 upstream gene variant A/C snv 0.62
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 1 2011 2011
dbSNP: rs3129871
rs3129871
0.827 0.320 6 32438565 upstream gene variant A/C snv 0.59
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 2 2007 2011
dbSNP: rs3129871
rs3129871
0.827 0.320 6 32438565 upstream gene variant A/C snv 0.59
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.800 1.000 2 2010 2013
dbSNP: rs3129871
rs3129871
0.827 0.320 6 32438565 upstream gene variant A/C snv 0.59
Diabetes Mellitus, Insulin-Dependent
0.700 1.000 1 2007 2007
dbSNP: rs3129871
rs3129871
0.827 0.320 6 32438565 upstream gene variant A/C snv 0.59
CUI: C0026691
Disease: Mucocutaneous Lymph Node Syndrome
Mucocutaneous Lymph Node Syndrome
0.700 1.000 1 2012 2012
dbSNP: rs3129871
rs3129871
0.827 0.320 6 32438565 upstream gene variant A/C snv 0.59
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma
0.700 1.000 1 2010 2010
dbSNP: rs3129872
rs3129872
0.925 0.160 6 32439376 upstream gene variant A/T snv 0.24
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1.000 1 2007 2007
dbSNP: rs3129872
rs3129872
0.925 0.160 6 32439376 upstream gene variant A/T snv 0.24
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 1 2011 2011
dbSNP: rs3129877
rs3129877
0.925 0.160 6 32440820 intron variant G/A snv 0.26
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 1 2011 2011
dbSNP: rs3129877
rs3129877
0.925 0.160 6 32440820 intron variant G/A snv 0.26
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1.000 1 2007 2007
dbSNP: rs3129878
rs3129878
0.807 0.360 6 32440958 intron variant A/C snv 0.30
CUI: C4021107
Disease: Non-obstructive azoospermia
Non-obstructive azoospermia
0.720 0.667 1 2012 2017
dbSNP: rs3129878
rs3129878
0.807 0.360 6 32440958 intron variant A/C snv 0.30
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 1 2011 2011
dbSNP: rs3129880
rs3129880
1.000 0.040 6 32441140 intron variant T/C snv 0.80
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
0.700 1.000 1 2012 2012
dbSNP: rs3129881
rs3129881
1.000 0.120 6 32441707 intron variant C/T snv 0.24
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 1 2011 2011
dbSNP: rs3129882
rs3129882
0.807 0.240 6 32441753 intron variant G/A snv 0.56
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 3 2007 2011
dbSNP: rs3129882
rs3129882
0.807 0.240 6 32441753 intron variant G/A snv 0.56
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.900 0.818 2 2010 2015
dbSNP: rs3129882
rs3129882
0.807 0.240 6 32441753 intron variant G/A snv 0.56
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma
0.800 1.000 1 2011 2011
dbSNP: rs3129882
rs3129882
0.807 0.240 6 32441753 intron variant G/A snv 0.56
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1.000 1 2010 2010
dbSNP: rs3129882
rs3129882
0.807 0.240 6 32441753 intron variant G/A snv 0.56
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease
0.700 1.000 1 2013 2013
dbSNP: rs3129883
rs3129883
0.925 0.160 6 32442360 intron variant T/C;G snv 0.74
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 1 2011 2011