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: rs3810936
rs3810936
TNFSF15
0.742 0.320 9 114790605 synonymous variant T/C snv 0.71 0.75
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.850 1.000 1 2005 2018
dbSNP: rs7848647
rs7848647
TNFSF15
0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.840 1.000 1 2005 2018
dbSNP: rs4979462
rs4979462
TNFSF15
0.790 0.240 9 114804733 intron variant C/T snv 0.13
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.830 1.000 3 2012 2019
dbSNP: rs4263839
rs4263839
TNFSF15
0.807 0.160 9 114804160 intron variant A/G snv 0.75
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.830 0.750 1 2008 2014
dbSNP: rs6478109
rs6478109
TNFSF15
0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.830 1.000 1 2005 2016
dbSNP: rs6478108
rs6478108
TNFSF15
0.763 0.200 9 114796423 intron variant C/T snv 0.73
CUI: C0023343
Disease: Leprosy
Leprosy 		0.810 1.000 1 2009 2016
dbSNP: rs4246905
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.800 1.000 3 2011 2015
dbSNP: rs4246905
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.800 1.000 1 2012 2012
dbSNP: rs6478109
rs6478109
TNFSF15
0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.800 1.000 1 2008 2008
dbSNP: rs7848647
rs7848647
TNFSF15
0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.730 1.000 1 2014 2018
dbSNP: rs7848647
rs7848647
TNFSF15
0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.710 1.000 1 2015 2018
dbSNP: rs7848647
rs7848647
TNFSF15
0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.710 0.500 1 2015 2016
dbSNP: rs4246905
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 2 2015 2015
dbSNP: rs4246905
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.700 1.000 1 2015 2015
dbSNP: rs4246905
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.700 1.000 1 2015 2015
dbSNP: rs4246905
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76
CUI: C0009447
Disease: Common Variable Immunodeficiency
Common Variable Immunodeficiency 		0.700 1.000 1 2015 2015
dbSNP: rs4246905
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 1.000 1 2015 2015
dbSNP: rs4246905
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0.700 1.000 1 2015 2015
dbSNP: rs4246905
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		0.700 1.000 1 2015 2015
dbSNP: rs4246905
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76
CUI: C0920350
Disease: Autoimmune thyroiditis
Autoimmune thyroiditis 		0.700 1.000 1 2015 2015
dbSNP: rs4246905
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		0.700 1.000 1 2015 2015
dbSNP: rs4246905
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76
CUI: C3495559
Disease: Juvenile arthritis
Juvenile arthritis 		0.700 1.000 1 2015 2015
dbSNP: rs4246905
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2015 2015
dbSNP: rs4246905
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.700 1.000 1 2015 2015
dbSNP: rs4246905
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2015 2015