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: rs1464510
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.810 1.000 3 2010 2015
dbSNP: rs1464510
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.800 1.000 2 2008 2010
dbSNP: rs1464510
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 2 2011 2011
dbSNP: rs1464510
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.700 1.000 1 2011 2011
dbSNP: rs1464510
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv
CUI: C0021053
Disease: Immune System Diseases
Immune System Diseases 		0.700 1.000 1 2011 2011
dbSNP: rs1464510
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.700 1.000 1 2011 2011
dbSNP: rs1464510
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2013 2013