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: rs492602
rs492602
FUT2 ; LOC105447645
0.925 0.120 19 48703160 synonymous variant A/G snv 0.38 0.45
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 3 2010 2018
dbSNP: rs516246
rs516246
FUT2 ; LOC105447645
0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 3 2012 2017
dbSNP: rs602662
rs602662
FUT2 ; LOC105447645
0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47
CUI: C0202252
Disease: VITAMIN B12 MEASUREMENT
VITAMIN B12 MEASUREMENT 		0.800 1.000 3 2009 2017
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: C0202252
Disease: VITAMIN B12 MEASUREMENT
VITAMIN B12 MEASUREMENT 		0.800 1.000 1 2012 2012
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: 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: 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: 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: C0010346
Disease: Crohn Disease
Crohn Disease 		0.710 1.000 1 2010 2015
dbSNP: rs492602
rs492602
FUT2 ; LOC105447645
0.925 0.120 19 48703160 synonymous variant A/G snv 0.38 0.45
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 2 2018 2019
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: rs35106244
rs35106244
FUT2
19 48700572 intron variant C/T snv 0.29
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
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: rs492602
rs492602
FUT2 ; LOC105447645
0.925 0.120 19 48703160 synonymous variant A/G snv 0.38 0.45
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs492602
rs492602
FUT2 ; LOC105447645
0.925 0.120 19 48703160 synonymous variant A/G snv 0.38 0.45
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2017 2017
dbSNP: rs492602
rs492602
FUT2 ; LOC105447645
0.925 0.120 19 48703160 synonymous variant A/G snv 0.38 0.45
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
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: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs516246
rs516246
FUT2 ; LOC105447645
0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs516246
rs516246
FUT2 ; LOC105447645
0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2018 2018
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: rs516246
rs516246
FUT2 ; LOC105447645
0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45
CUI: C0005612
Disease: Birth Weight
Birth Weight 		0.700 1.000 1 2019 2019
dbSNP: rs516246
rs516246
FUT2 ; LOC105447645
0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs516246
rs516246
FUT2 ; LOC105447645
0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018