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: rs66803065
rs66803065
SBF2
11 10004305 intron variant C/A;T snv 0.19
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2017 2017
dbSNP: rs66803065
rs66803065
SBF2
11 10004305 intron variant C/A;T snv 0.19
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2017 2017
dbSNP: rs11042561
rs11042561
SBF2
0.925 0.040 11 9941510 intron variant C/A snv 0.20
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 1.000 1 2018 2018
dbSNP: rs11042561
rs11042561
SBF2
0.925 0.040 11 9941510 intron variant C/A snv 0.20
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs10840349
rs10840349
SBF2
11 10054883 intron variant A/G;T snv
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs11042549
rs11042549
SBF2 ; LOC101928008
1.000 0.040 11 9927031 intron variant A/G;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs11042543
rs11042543
SBF2 ; LOC101928008
1.000 0.040 11 9918271 intron variant A/G snv 0.20
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs55893317
rs55893317
SBF2
11 10159444 intron variant A/G snv 0.25
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs4450168
rs4450168
SBF2
0.790 0.080 11 10265208 intron variant A/C;T snv 0.12
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2019 2019
dbSNP: rs4450168
rs4450168
SBF2
0.790 0.080 11 10265208 intron variant A/C;T snv 0.12
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 1.000 1 2019 2019
dbSNP: rs4450168
rs4450168
SBF2
0.790 0.080 11 10265208 intron variant A/C;T snv 0.12
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2019 2019
dbSNP: rs4450168
rs4450168
SBF2
0.790 0.080 11 10265208 intron variant A/C;T snv 0.12
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.700 1.000 1 2019 2019
dbSNP: rs4450168
rs4450168
SBF2
0.790 0.080 11 10265208 intron variant A/C;T snv 0.12
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		0.700 1.000 1 2019 2019
dbSNP: rs4450168
rs4450168
SBF2
0.790 0.080 11 10265208 intron variant A/C;T snv 0.12
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2019 2019
dbSNP: rs4450168
rs4450168
SBF2
0.790 0.080 11 10265208 intron variant A/C;T snv 0.12
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 1 2019 2019
dbSNP: rs4450168
rs4450168
SBF2
0.790 0.080 11 10265208 intron variant A/C;T snv 0.12
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		0.700 1.000 1 2019 2019
dbSNP: rs4450168
rs4450168
SBF2
0.790 0.080 11 10265208 intron variant A/C;T snv 0.12
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.700 1.000 1 2019 2019