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: rs872071
rs872071
IRF4
0.742 0.360 6 411064 3 prime UTR variant A/G;T snv
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		0.840 1.000 4 2008 2014
dbSNP: rs12203592
rs12203592
IRF4
0.649 0.320 6 396321 intron variant C/T snv 0.10
CUI: C0018498
Disease: Hair Color
Hair Color 		0.800 1.000 3 2008 2013
dbSNP: rs1050976
rs1050976
IRF4
0.851 0.280 6 408079 3 prime UTR variant C/T snv 0.37
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.800 1.000 1 2011 2011
dbSNP: rs12203592
rs12203592
IRF4
0.649 0.320 6 396321 intron variant C/T snv 0.10
CUI: C0015396
Disease: Eye Color
Eye Color 		0.800 1.000 1 2010 2018
dbSNP: rs12203592
rs12203592
IRF4
0.649 0.320 6 396321 intron variant C/T snv 0.10
CUI: C0038868
Disease: Progressive supranuclear palsy
Progressive supranuclear palsy 		0.800 1.000 1 2011 2011
dbSNP: rs1050976
rs1050976
IRF4
0.851 0.280 6 408079 3 prime UTR variant C/T snv 0.37
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		0.700 1.000 1 2013 2013
dbSNP: rs12203592
rs12203592
IRF4
0.649 0.320 6 396321 intron variant C/T snv 0.10
CUI: C0016689
Disease: Freckles
Freckles 		0.700 1.000 1 2010 2010
dbSNP: rs12203592
rs12203592
IRF4
0.649 0.320 6 396321 intron variant C/T snv 0.10
CUI: C0699893
Disease: Skin carcinoma
Skin carcinoma 		0.700 1.000 1 2013 2013
dbSNP: rs872071
rs872071
IRF4
0.742 0.360 6 411064 3 prime UTR variant A/G;T snv
CUI: C0242350
Disease: Erectile dysfunction
Erectile dysfunction 		0.700 1.000 1 2012 2012
dbSNP: rs872071
rs872071
IRF4
0.742 0.360 6 411064 3 prime UTR variant A/G;T snv
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		0.700 1.000 1 2010 2010