Source: GWASCAT

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: rs11879191
rs11879191
CDC37
1.000 0.040 19 10402235 intron variant G/A;C snv
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.800 1.000 2 2012 2017
dbSNP: rs8112449
rs8112449
CDC37
0.925 0.160 19 10409388 intron variant G/A snv 0.31
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.800 1.000 1 2011 2011
dbSNP: rs11879191
rs11879191
CDC37
1.000 0.040 19 10402235 intron variant G/A;C snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 2 2015 2017
dbSNP: rs35164067
rs35164067
CDC37
1.000 0.040 19 10414505 intron variant G/A snv 0.18
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2013 2013
dbSNP: rs35164067
rs35164067
CDC37
1.000 0.040 19 10414505 intron variant G/A snv 0.18
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.700 1.000 1 2015 2015