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: rs504963
rs504963
FUT2 ; LOC105447645
1.000 0.040 19 48705608 3 prime UTR variant G/A snv 0.48
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2010 2010
dbSNP: rs281377
rs281377
FUT2 ; LOC105447645
0.925 0.120 19 48703346 synonymous variant C/T snv 0.49 0.42
CUI: C0201850
Disease: Alkaline phosphatase measurement
Alkaline phosphatase measurement 		0.800 1.000 1 2011 2011
dbSNP: rs516246
rs516246
FUT2 ; LOC105447645
0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45
CUI: C1278049
Disease: Serum gamma-glutamyl transferase measurement
Serum gamma-glutamyl transferase measurement 		0.800 1.000 1 2011 2011
dbSNP: rs1047781
rs1047781
FUT2 ; LOC105447645
0.790 0.200 19 48703374 missense variant A/T snv 3.6E-02 1.2E-02
CUI: C0202252
Disease: VITAMIN B12 MEASUREMENT
VITAMIN B12 MEASUREMENT 		0.800 1.000 1 2012 2012
dbSNP: rs492602
rs492602
FUT2 ; LOC105447645
0.925 0.120 19 48703160 synonymous variant A/G snv 0.38 0.45
CUI: C0202252
Disease: VITAMIN B12 MEASUREMENT
VITAMIN B12 MEASUREMENT 		0.800 1.000 2 2008 2014
dbSNP: rs1047781
rs1047781
FUT2 ; LOC105447645
0.790 0.200 19 48703374 missense variant A/T snv 3.6E-02 1.2E-02
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2015 2015
dbSNP: rs516246
rs516246
FUT2 ; LOC105447645
0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.700 1.000 1 2015 2015
dbSNP: rs516246
rs516246
FUT2 ; LOC105447645
0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.700 1.000 1 2015 2015
dbSNP: rs602662
rs602662
FUT2 ; LOC105447645
0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2015 2015
dbSNP: rs602662
rs602662
FUT2 ; LOC105447645
0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47
CUI: C3495559
Disease: Juvenile arthritis
Juvenile arthritis 		0.700 1.000 1 2015 2015
dbSNP: rs602662
rs602662
FUT2 ; LOC105447645
0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47
CUI: C0009447
Disease: Common Variable Immunodeficiency
Common Variable Immunodeficiency 		0.700 1.000 1 2015 2015
dbSNP: rs602662
rs602662
FUT2 ; LOC105447645
0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.700 1.000 1 2015 2015
dbSNP: rs602662
rs602662
FUT2 ; LOC105447645
0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		0.700 1.000 1 2015 2015
dbSNP: rs602662
rs602662
FUT2 ; LOC105447645
0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.700 1.000 1 2015 2015
dbSNP: rs602662
rs602662
FUT2 ; LOC105447645
0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.710 1.000 1 2012 2015
dbSNP: rs602662
rs602662
FUT2 ; LOC105447645
0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		0.700 1.000 1 2015 2015
dbSNP: rs602662
rs602662
FUT2 ; LOC105447645
0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0.700 1.000 1 2015 2015
dbSNP: rs602662
rs602662
FUT2 ; LOC105447645
0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 1.000 1 2015 2015
dbSNP: rs602662
rs602662
FUT2 ; LOC105447645
0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.710 1.000 1 2010 2015
dbSNP: rs602662
rs602662
FUT2 ; LOC105447645
0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2015 2015
dbSNP: rs602662
rs602662
FUT2 ; LOC105447645
0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47
CUI: C0920350
Disease: Autoimmune thyroiditis
Autoimmune thyroiditis 		0.700 1.000 1 2015 2015
dbSNP: rs602662
rs602662
FUT2 ; LOC105447645
0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.700 1.000 1 2015 2015
dbSNP: rs35106244
rs35106244
FUT2
19 48700572 intron variant C/T snv 0.29
CUI: C0011991
Disease: Diarrhea
Diarrhea 		0.700 1.000 1 2016 2016
dbSNP: rs679574
rs679574
FUT2 ; LOC105447645
0.827 0.120 19 48702851 intron variant C/G snv 0.45
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2016 2016
dbSNP: rs679574
rs679574
FUT2 ; LOC105447645
0.827 0.120 19 48702851 intron variant C/G snv 0.45
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016