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: rs2514218
rs2514218 		0.925 0.040 11 113522272 regulatory region variant C/T snv 0.26
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.740 1.000 7 2014 2019
dbSNP: rs7405404
rs7405404 		0.925 0.040 16 13656002 intergenic variant T/A;C snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 7 2014 2019
dbSNP: rs7801375
rs7801375 		1.000 0.040 7 131882504 intergenic variant A/G snv 0.73
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 7 2014 2019
dbSNP: rs9540493
rs9540493 		1.000 0.040 13 65631572 intergenic variant A/G snv 0.49
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 7 2015 2019
dbSNP: rs11165643
rs11165643 		1 96458541 intergenic variant C/T snv 0.48
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 6 2015 2019
dbSNP: rs11953630
rs11953630 		5 158418394 intergenic variant C/A;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 6 2011 2018
dbSNP: rs13209747
rs13209747 		6 126794309 intron variant C/G;T snv 0.36
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 6 2013 2018
dbSNP: rs16892766
rs16892766 		0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		0.700 1.000 6 2008 2019
dbSNP: rs16892766
rs16892766 		0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 6 2008 2019
dbSNP: rs16892766
rs16892766 		0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		0.700 1.000 6 2008 2019
dbSNP: rs16892766
rs16892766 		0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.900 1.000 6 2008 2019
dbSNP: rs16892766
rs16892766 		0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 6 2008 2019
dbSNP: rs16892766
rs16892766 		0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 6 2008 2019
dbSNP: rs16892766
rs16892766 		0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.710 1.000 6 2008 2019
dbSNP: rs16892766
rs16892766 		0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.700 1.000 6 2008 2019
dbSNP: rs16892766
rs16892766 		0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 6 2008 2019
dbSNP: rs16907751
rs16907751 		8 80463222 intron variant C/T snv 0.10
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 6 2015 2019
dbSNP: rs16998073
rs16998073 		0.925 0.120 4 80263187 upstream gene variant A/G;T snv
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 6 2009 2019
dbSNP: rs17085007
rs17085007 		0.827 0.120 13 26957130 regulatory region variant T/C snv 0.16
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.820 1.000 6 2009 2017
dbSNP: rs2068888
rs2068888 		10 93079885 downstream gene variant G/A snv 0.42
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 6 2010 2019
dbSNP: rs2954029
rs2954029 		0.807 0.160 8 125478730 intron variant A/T snv 0.42
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 6 2010 2019
dbSNP: rs29941
rs29941 		1.000 0.080 19 33818627 downstream gene variant A/G snv 0.70
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 6 2009 2018
dbSNP: rs35444
rs35444 		12 115114632 intergenic variant A/G snv 0.38
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 6 2011 2019
dbSNP: rs3764261
rs3764261 		0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 6 2010 2019
dbSNP: rs439401
rs439401 		0.851 0.200 19 44911194 non coding transcript exon variant T/C snv 0.68
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 6 2009 2019