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: rs2366643
rs2366643
LINC01100 ; IL12A-AS1
1.000 0.080 3 160018698 intron variant T/C;G snv
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.800 1.000 1 2012 2012
dbSNP: rs2243112
rs2243112
IL12A ; IL12A-AS1
3 159987881 intron variant G/C snv 5.7E-03
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2243112
rs2243112
IL12A ; IL12A-AS1
3 159987881 intron variant G/C snv 5.7E-03
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2243112
rs2243112
IL12A ; IL12A-AS1
3 159987881 intron variant G/C snv 5.7E-03
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1874886
rs1874886
IL12A-AS1
0.925 0.280 3 160011868 non coding transcript exon variant G/A snv 0.41
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.700 1.000 1 2012 2012
dbSNP: rs17810546
rs17810546
IL12A-AS1
0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.820 1.000 2 2008 2020
dbSNP: rs17810546
rs17810546
IL12A-AS1
0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.810 1.000 1 2013 2015
dbSNP: rs17810546
rs17810546
IL12A-AS1
0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.700 1.000 1 2011 2011
dbSNP: rs17810546
rs17810546
IL12A-AS1
0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2011 2011
dbSNP: rs17810546
rs17810546
IL12A-AS1
0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.700 1.000 1 2011 2011
dbSNP: rs17810546
rs17810546
IL12A-AS1
0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02
CUI: C0021053
Disease: Immune System Diseases
Immune System Diseases 		0.700 1.000 1 2011 2011
dbSNP: rs1651081
rs1651081
IL12A-AS1
1.000 0.080 3 160014715 intron variant A/T snv 0.41
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.700 1.000 1 2012 2012
dbSNP: rs1353248
rs1353248
IL12A-AS1
0.925 0.120 3 159905770 intron variant C/T snv 0.32
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.800 1.000 1 2011 2011
dbSNP: rs11918142
rs11918142
IL12A-AS1
1.000 0.040 3 160189298 intron variant T/C snv 0.20
CUI: C4021107
Disease: Non-obstructive azoospermia
Non-obstructive azoospermia 		0.700 1.000 1 2011 2011