Source: GWASDB

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: rs653178
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.810 1.000 2 2008 2011
dbSNP: rs3184504
rs3184504
ATXN2 ; SH2B3
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C1305849
Disease: Diastolic blood pressure measurement
Diastolic blood pressure measurement 		0.700 1.000 3 2009 2013
dbSNP: rs3184504
rs3184504
ATXN2 ; SH2B3
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C1306620
Disease: Systolic blood pressure measurement
Systolic blood pressure measurement 		0.700 1.000 2 2009 2013
dbSNP: rs3184504
rs3184504
ATXN2 ; SH2B3
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.820 1.000 2 2009 2018
dbSNP: rs10774625
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2009 2009
dbSNP: rs3184504
rs3184504
ATXN2 ; SH2B3
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.800 1.000 1 2009 2016
dbSNP: rs3184504
rs3184504
ATXN2 ; SH2B3
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.800 1.000 1 2009 2019
dbSNP: rs4766578
rs4766578
ATXN2
0.851 0.200 12 111466567 intron variant T/A snv 0.66
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2009 2009
dbSNP: rs653178
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2009 2009
dbSNP: rs653178
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67
CUI: C1305849
Disease: Diastolic blood pressure measurement
Diastolic blood pressure measurement 		0.700 1.000 1 2009 2009
dbSNP: rs653178
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases 		0.700 1.000 1 2010 2010
dbSNP: rs3184504
rs3184504
ATXN2 ; SH2B3
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.800 1.000 2 2011 2016
dbSNP: rs653178
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 2 2011 2011
dbSNP: rs3184504
rs3184504
ATXN2 ; SH2B3
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0021053
Disease: Immune System Diseases
Immune System Diseases 		0.700 1.000 1 2011 2011
dbSNP: rs3184504
rs3184504
ATXN2 ; SH2B3
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.810 1.000 1 2011 2015
dbSNP: rs3184504
rs3184504
ATXN2 ; SH2B3
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.700 1.000 1 2011 2011
dbSNP: rs3184504
rs3184504
ATXN2 ; SH2B3
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C1272321
Disease: Autoantibody measurement
Autoantibody measurement 		0.800 1.000 1 2011 2018
dbSNP: rs3184504
rs3184504
ATXN2 ; SH2B3
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011
dbSNP: rs3184504
rs3184504
ATXN2 ; SH2B3
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.820 1.000 1 2011 2018
dbSNP: rs653178
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.700 1.000 1 2011 2011
dbSNP: rs653178
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2011 2011
dbSNP: rs653178
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.800 1.000 1 2011 2011
dbSNP: rs653178
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67
CUI: C0021053
Disease: Immune System Diseases
Immune System Diseases 		0.800 1.000 1 2011 2011
dbSNP: rs653178
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.710 1.000 1 2011 2013
dbSNP: rs739496
rs739496
ATXN2 ; SH2B3
0.790 0.160 12 111449855 3 prime UTR variant A/G snv 0.27
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.700 1.000 1 2011 2011