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: rs7903146
rs7903146
0.554 0.680 10 112998590 intron variant C/G;T snv
Diabetes Mellitus, Non-Insulin-Dependent
0.900 0.953 28 2006 2020
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 20 2009 2019
dbSNP: rs3764261
rs3764261
0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31
High density lipoprotein measurement
0.800 1.000 19 2008 2019
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: rs4420638
rs4420638
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18
Low density lipoprotein cholesterol measurement
0.800 1.000 14 2007 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
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
0.730 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, 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
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.770 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
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.900 0.945 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: rs6511720
rs6511720
0.790 0.120 19 11091630 intron variant G/T snv 0.12
Low density lipoprotein cholesterol measurement
0.800 1.000 12 2008 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: rs10993994
rs10993994
0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.800 1.000 11 2008 2020
dbSNP: rs12678919
rs12678919
0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 11 2009 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: rs2954029
rs2954029
0.807 0.160 8 125478730 intron variant A/T snv 0.42
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 11 2009 2019
dbSNP: rs3803662
rs3803662
0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.900 0.953 11 2007 2019
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
High density lipoprotein measurement
0.800 1.000 11 2009 2019
dbSNP: rs10811661
rs10811661
0.724 0.400 9 22134095 intergenic variant T/C snv 0.14
Diabetes Mellitus, Non-Insulin-Dependent
0.900 0.955 10 2007 2019