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: rs2024092
rs2024092
SBNO2
0.827 0.120 19 1124032 intron variant G/A snv 0.24 0.26
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 2 2008 2017
dbSNP: rs740495
rs740495
SBNO2
1.000 0.040 19 1124836 intron variant A/C;G snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2010 2010
dbSNP: rs4807569
rs4807569
SBNO2
0.925 0.120 19 1123379 intron variant A/C snv 0.25
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.710 1.000 1 2008 2010
dbSNP: rs4807569
rs4807569
SBNO2
0.925 0.120 19 1123379 intron variant A/C snv 0.25
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.700 1.000 1 2011 2011