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: rs2220970
rs2220970
SBF2
11 9836202 intron variant G/A snv 0.80
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 2 2018 2019
dbSNP: rs10500715
rs10500715
SBF2
0.925 0.120 11 9951515 intron variant T/G snv 0.39
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma 		0.700 1.000 1 2014 2014
dbSNP: rs10734650
rs10734650
SBF2
0.925 0.080 11 9820944 intron variant C/T snv 0.83
CUI: C2931384
Disease: Moyamoya disease 1
Moyamoya disease 1 		0.700 1.000 1 2018 2018
dbSNP: rs10734650
rs10734650
SBF2
0.925 0.080 11 9820944 intron variant C/T snv 0.83
CUI: C0026654
Disease: Moyamoya Disease
Moyamoya Disease 		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: 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: 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: 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: rs11042662
rs11042662
SBF2
11 10193627 intron variant C/T snv 0.27
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs117518788
rs117518788
SBF2
11 9980672 intron variant C/T snv 2.9E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs12361687
rs12361687
SBF2 ; LOC101928008
11 9868505 intron variant G/A snv 0.27
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs12362504
rs12362504
SBF2 ; LOC101928008
0.925 0.120 11 9907995 intron variant T/C snv 0.37
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma 		0.700 1.000 1 2017 2017
dbSNP: rs1372812
rs1372812
SBF2
0.925 0.040 11 10233236 intron variant T/C snv 2.2E-02
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 1.000 1 2018 2018
dbSNP: rs1372812
rs1372812
SBF2
0.925 0.040 11 10233236 intron variant T/C snv 2.2E-02
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs1470260
rs1470260
SBF2
11 10253573 intron variant T/C snv 0.20
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs17368443
rs17368443
SBF2
11 10275289 intron variant G/C snv 5.3E-02
CUI: C0001925
Disease: Albuminuria
Albuminuria 		0.700 1.000 1 2018 2018
dbSNP: rs360124
rs360124
SBF2 ; SBF2-AS1 ; LOC105369149
11 9780681 non coding transcript exon variant G/C snv 0.88
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs418635
rs418635
SBF2 ; SBF2-AS1
0.925 0.040 11 9796458 intron variant T/C snv 6.6E-02
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 1.000 1 2018 2018
dbSNP: rs418635
rs418635
SBF2 ; SBF2-AS1
0.925 0.040 11 9796458 intron variant T/C snv 6.6E-02
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs4323860
rs4323860
SBF2
11 10138336 intron variant T/C snv 0.50
CUI: C0005890
Disease: Body Height
Body Height 		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: 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