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: rs548234
rs548234
0.763 0.360 6 106120159 intron variant C/T snv 0.76
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.830 1.000 1 2009 2017
dbSNP: rs3827644
rs3827644
0.925 0.080 6 106237320 intron variant G/C snv 0.15
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma
0.800 1.000 1 2013 2013
dbSNP: rs6568431
rs6568431
0.790 0.320 6 106140931 intron variant A/C snv 0.61
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.800 1.000 1 2008 2017
dbSNP: rs6911490
rs6911490
1.000 0.040 6 106074152 intron variant T/C snv 0.86
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.800 1.000 1 2011 2011
dbSNP: rs9372120
rs9372120
0.851 0.280 6 106219660 intron variant T/G snv 0.16
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.800 1.000 1 2014 2019
dbSNP: rs573775
rs573775
0.851 0.320 6 106316991 intron variant G/A snv 0.34
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.720 1.000 1 2008 2018
dbSNP: rs538557
rs538557
1.000 0.080 6 106236001 intron variant T/C snv 4.3E-02
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs548234
rs548234
0.763 0.360 6 106120159 intron variant C/T snv 0.76
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
0.700 1.000 1 2011 2011
dbSNP: rs548234
rs548234
0.763 0.360 6 106120159 intron variant C/T snv 0.76
CUI: C0021053
Disease: Immune System Diseases
Immune System Diseases
0.700 1.000 1 2011 2011
dbSNP: rs548234
rs548234
0.763 0.360 6 106120159 intron variant C/T snv 0.76
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1.000 1 2011 2011
dbSNP: rs6568431
rs6568431
0.790 0.320 6 106140931 intron variant A/C snv 0.61
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1.000 1 2011 2011