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: rs204999
rs204999 		0.763 0.480 6 32142202 intergenic variant A/G snv 0.28
CUI: C0152268
Disease: Nodular Sclerosis Classical Hodgkin Lymphoma
Nodular Sclerosis Classical Hodgkin Lymphoma 		0.810 1.000 1 2012 2012
dbSNP: rs204999
rs204999 		0.763 0.480 6 32142202 intergenic variant A/G snv 0.28
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 2 2007 2011
dbSNP: rs204999
rs204999 		0.763 0.480 6 32142202 intergenic variant A/G snv 0.28
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease 		0.700 1.000 1 2014 2014
dbSNP: rs204999
rs204999 		0.763 0.480 6 32142202 intergenic variant A/G snv 0.28
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2013 2013
dbSNP: rs204999
rs204999 		0.763 0.480 6 32142202 intergenic variant A/G snv 0.28
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.700 1.000 1 2011 2011
dbSNP: rs204999
rs204999 		0.763 0.480 6 32142202 intergenic variant A/G snv 0.28
CUI: C0149678
Disease: Epstein-Barr Virus Infections
Epstein-Barr Virus Infections 		0.700 1.000 1 2013 2013
dbSNP: rs204999
rs204999 		0.763 0.480 6 32142202 intergenic variant A/G snv 0.28
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.700 1.000 1 2007 2007
dbSNP: rs204999
rs204999 		0.763 0.480 6 32142202 intergenic variant A/G snv 0.28
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2013 2013
dbSNP: rs204999
rs204999 		0.763 0.480 6 32142202 intergenic variant A/G snv 0.28
CUI: C0036836
Disease: Serum total protein measurement
Serum total protein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs204999
rs204999 		0.763 0.480 6 32142202 intergenic variant A/G snv 0.28
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.700 1.000 1 2013 2013
dbSNP: rs204999
rs204999 		0.763 0.480 6 32142202 intergenic variant A/G snv 0.28
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2012 2012
dbSNP: rs204999
rs204999 		0.763 0.480 6 32142202 intergenic variant A/G snv 0.28
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		0.700 1.000 1 2010 2010