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: rs17810546
rs17810546
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
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
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
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: rs17810546
rs17810546
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
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