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: rs2239804
rs2239804
0.851 0.240 6 32443746 intron variant T/A;C snv 0.51
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
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
Diabetes Mellitus, Insulin-Dependent
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: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1.000 1 2007 2007
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: rs3135392
rs3135392
0.925 0.160 6 32441465 intron variant C/A snv 0.38
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1.000 1 2007 2007
dbSNP: rs3177928
rs3177928
0.882 0.120 6 32444658 3 prime UTR variant G/A snv 0.13
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1.000 1 2007 2007
dbSNP: rs7194
rs7194
0.827 0.280 6 32444703 3 prime UTR variant G/A snv 0.61
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1.000 1 2007 2007
dbSNP: rs9268645
rs9268645
0.827 0.360 6 32440750 intron variant C/G;T snv
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1.000 1 2007 2007
dbSNP: rs7194
rs7194
0.827 0.280 6 32444703 3 prime UTR variant G/A snv 0.61
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs9268645
rs9268645
0.827 0.360 6 32440750 intron variant C/G;T snv
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs9268645
rs9268645
0.827 0.360 6 32440750 intron variant C/G;T snv
Diabetes Mellitus, Insulin-Dependent
0.800 1.000 1 2009 2009
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: 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: 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: rs2239804
rs2239804
0.851 0.240 6 32443746 intron variant T/A;C snv 0.51
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
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: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 3 2007 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: rs7192
rs7192
0.827 0.200 6 32443869 missense variant T/G snv 0.64 0.61
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 2 2007 2011
dbSNP: rs1041885
rs1041885
1.000 0.120 6 32445032 3 prime UTR variant T/A snv 0.15
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 1 2011 2011
dbSNP: rs1051336
rs1051336
0.925 0.120 6 32444815 3 prime UTR variant G/A;C snv 0.15
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 1 2011 2011
dbSNP: rs14004
rs14004
1.000 0.120 6 32439932 5 prime UTR variant C/A snv 0.44 0.39
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 1 2011 2011
dbSNP: rs2239802
rs2239802
0.882 0.200 6 32444069 intron variant C/A;G;T snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 1 2011 2011
dbSNP: rs2239803
rs2239803
0.882 0.240 6 32444056 intron variant C/A;T snv 0.50
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 1 2011 2011