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: rs10938397
rs10938397
0.851 0.200 4 45180510 intergenic variant A/G snv 0.37
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 14 2009 2019
dbSNP: rs543874
rs543874
1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 14 2010 2019
dbSNP: rs6983267
rs6983267
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 14 2007 2019
dbSNP: rs6983267
rs6983267
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
0.700 1.000 14 2007 2019
dbSNP: rs6983267
rs6983267
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
Malignant neoplasm of large intestine
0.700 1.000 14 2007 2019
dbSNP: rs6983267
rs6983267
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
0.700 1.000 14 2007 2019
dbSNP: rs6983267
rs6983267
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
0.700 1.000 14 2007 2019
dbSNP: rs6983267
rs6983267
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.700 1.000 14 2007 2019
dbSNP: rs6567160
rs6567160
1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 12 2014 2019
dbSNP: rs7138803
rs7138803
0.827 0.240 12 49853685 intergenic variant G/A;T snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 12 2009 2019
dbSNP: rs13107325
rs13107325
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 11 2010 2019
dbSNP: rs1558902
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 11 2010 2019
dbSNP: rs12429545
rs12429545
13 53528071 intron variant G/A;T snv 0.12
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 10 2015 2019
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 10 2009 2019
dbSNP: rs3810291
rs3810291
19 47065746 3 prime UTR variant G/A snv 0.50
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 10 2010 2019
dbSNP: rs1458038
rs1458038
0.925 0.120 4 80243569 intergenic variant C/T snv 0.23
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 9 2011 2019
dbSNP: rs1458038
rs1458038
0.925 0.120 4 80243569 intergenic variant C/T snv 0.23
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 9 2011 2019
dbSNP: rs2112347
rs2112347
0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 9 2010 2019
dbSNP: rs880315
rs880315
0.925 0.120 1 10736809 intron variant T/C snv 0.32
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 9 2011 2018
dbSNP: rs9895661
rs9895661
0.882 0.200 17 61379228 non coding transcript exon variant C/T snv 0.69
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 9 2016 2019
dbSNP: rs10182181
rs10182181
1.000 0.080 2 24927427 intergenic variant A/G snv 0.57
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 8 2015 2019
dbSNP: rs11191548
rs11191548
0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 8 2009 2018
dbSNP: rs13021737
rs13021737
2 632348 intergenic variant A/G snv 0.85
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 8 2015 2019
dbSNP: rs13107325
rs13107325
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 8 2011 2019
dbSNP: rs17249754
rs17249754
0.882 0.120 12 89666809 intron variant G/A snv 0.15
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 8 2009 2018