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: rs11712165
rs11712165
ARHGAP31
0.882 0.200 3 119399949 intron variant T/G snv 0.30
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.800 1.000 1 2010 2010
dbSNP: rs11712165
rs11712165
ARHGAP31
0.882 0.200 3 119399949 intron variant T/G snv 0.30
CUI: C0021053
Disease: Immune System Diseases
Immune System Diseases 		0.700 1.000 1 2011 2011
dbSNP: rs11712165
rs11712165
ARHGAP31
0.882 0.200 3 119399949 intron variant T/G snv 0.30
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.700 1.000 1 2011 2011
dbSNP: rs11712165
rs11712165
ARHGAP31
0.882 0.200 3 119399949 intron variant T/G snv 0.30
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.700 1.000 1 2011 2011
dbSNP: rs11712165
rs11712165
ARHGAP31
0.882 0.200 3 119399949 intron variant T/G snv 0.30
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2011 2011