Source: GWASDB ×
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2066845
rs2066845 		0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 1.000 0.949 3 2001 2019
dbSNP: rs2066844
rs2066844 		0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 1.000 0.940 2 2001 2018
dbSNP: rs2066847
rs2066847 		0.716 0.400 16 50729868 frameshift variant C/-;CC delins 1.5E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.890 0.923 4 2005 2019
dbSNP: rs2076756
rs2076756 		0.882 0.040 16 50722970 intron variant A/G snv 0.17
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.830 1.000 6 2007 2019
dbSNP: rs5743293
rs5743293 		0.807 0.200 16 50729868 frameshift variant C/-;CC delins
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.830 1.000 4 2007 2017
dbSNP: rs2076756
rs2076756 		0.882 0.040 16 50722970 intron variant A/G snv 0.17
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		Digestive System Diseases 0.820 1.000 1 2006 2017
dbSNP: rs17221417
rs17221417 		0.925 0.040 16 50705671 intron variant C/G snv 0.20
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.810 1.000 2 2007 2017
dbSNP: rs5743289
rs5743289 		1.000 0.040 16 50722863 intron variant C/G;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.810 1.000 2 2007 2014
dbSNP: rs5743289
rs5743289 		1.000 0.040 16 50722863 intron variant C/G;T snv
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		Digestive System Diseases 0.800 1.000 1 2008 2008
dbSNP: rs2066842
rs2066842 		0.763 0.200 16 50710713 missense variant C/A;T snv 4.0E-06; 0.19
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.790 1.000 1 2002 2014
dbSNP: rs17313265
rs17313265 		1.000 0.040 16 50713793 intron variant C/T snv 0.20
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.710 1.000 1 2007 2014
dbSNP: rs2066843
rs2066843 		0.925 0.040 16 50711288 synonymous variant C/A;T snv 0.19
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.710 1.000 1 2006 2010
dbSNP: rs5743291
rs5743291 		0.925 0.040 16 50723365 missense variant G/A snv 6.3E-02 6.0E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.710 1.000 1 2007 2008
dbSNP: rs199883290
rs199883290 		0.925 0.120 16 50729867 missense variant G/A;C snv 4.0E-06; 1.5E-02 7.0E-06
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 4 2007 2012
dbSNP: rs540973741
rs540973741 		0.925 0.120 16 50729868 frameshift variant C/-;CC delins
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 4 2007 2012
dbSNP: rs17312836
rs17312836 		1.000 0.040 16 50707551 intron variant A/C snv 0.33
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 1 2007 2007
dbSNP: rs199883290
rs199883290 		0.925 0.120 16 50729867 missense variant G/A;C snv 4.0E-06; 1.5E-02 7.0E-06
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs2066847
rs2066847 		0.716 0.400 16 50729868 frameshift variant C/-;CC delins 1.5E-02
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs2076753
rs2076753 		1.000 0.040 16 50699463 intron variant G/A;T snv 0.20
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 1 2007 2007
dbSNP: rs3135499
rs3135499 		0.882 0.160 16 50732216 splice donor variant A/C snv 0.45
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 1 2007 2007
dbSNP: rs540973741
rs540973741 		0.925 0.120 16 50729868 frameshift variant C/-;CC delins
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs5743293
rs5743293 		0.807 0.200 16 50729868 frameshift variant C/-;CC delins
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs749910
rs749910 		1.000 0.040 16 50724938 intron variant G/A snv 0.17
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 1 2007 2007
dbSNP: rs751271
rs751271 		1.000 0.040 16 50717264 intron variant T/G snv 0.61
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 1 2007 2007
dbSNP: rs8056611
rs8056611 		1.000 0.040 16 50733736 3 prime UTR variant A/G snv 0.56
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 1 2007 2007