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: rs2523946
rs2523946
HLA-A ; HCG9
0.925 0.200 6 29974166 upstream gene variant C/A;G;T snv
CUI: C0017661
Disease: IGA Glomerulonephritis
IGA Glomerulonephritis 		0.800 1.000 1 2011 2015
dbSNP: rs3823355
rs3823355
HLA-A ; HCG9
1.000 0.040 6 29974306 upstream gene variant C/A;T snv
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.800 1.000 1 2010 2010
dbSNP: rs2523946
rs2523946
HLA-A ; HCG9
0.925 0.200 6 29974166 upstream gene variant C/A;G;T snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 2 2007 2009
dbSNP: rs3132685
rs3132685
HLA-A ; HCG9
0.807 0.320 6 29978172 intron variant G/A;T snv
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		0.700 1.000 2 2009 2012
dbSNP: rs6904029
rs6904029
HLA-A ; HCG9
0.851 0.200 6 29975290 non coding transcript exon variant G/A snv 0.29 0.26
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 2 2007 2009
dbSNP: rs2735076
rs2735076
HLA-A ; HCG9
1.000 0.040 6 29975713 intron variant A/G snv 0.71
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2012 2012
dbSNP: rs2735076
rs2735076
HLA-A ; HCG9
1.000 0.040 6 29975713 intron variant A/G snv 0.71
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs3132685
rs3132685
HLA-A ; HCG9
0.807 0.320 6 29978172 intron variant G/A;T snv
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 1.000 1 2014 2014
dbSNP: rs3132685
rs3132685
HLA-A ; HCG9
0.807 0.320 6 29978172 intron variant G/A;T snv
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.700 1.000 1 2007 2007
dbSNP: rs3132685
rs3132685
HLA-A ; HCG9
0.807 0.320 6 29978172 intron variant G/A;T snv
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis 		0.700 1.000 1 2012 2012
dbSNP: rs3132685
rs3132685
HLA-A ; HCG9
0.807 0.320 6 29978172 intron variant G/A;T snv
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		0.700 1.000 1 2009 2009
dbSNP: rs6904029
rs6904029
HLA-A ; HCG9
0.851 0.200 6 29975290 non coding transcript exon variant G/A snv 0.29 0.26
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.700 1.000 1 2010 2010