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: rs1144700
rs1144700
ATXN1
6 16744456 intron variant C/G;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 2 2016 2019
dbSNP: rs73366713
rs73366713
ATXN1
1.000 0.080 6 16415520 intron variant G/A;T snv
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.700 1.000 2 2018 2018
dbSNP: rs1144700
rs1144700
ATXN1
6 16744456 intron variant C/G;T snv
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs1144700
rs1144700
ATXN1
6 16744456 intron variant C/G;T snv
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		0.700 1.000 1 2016 2016
dbSNP: rs1144700
rs1144700
ATXN1
6 16744456 intron variant C/G;T snv
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs1144700
rs1144700
ATXN1
6 16744456 intron variant C/G;T snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs1322599
rs1322599
ATXN1
6 16758194 intron variant C/T snv 0.20
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2018 2018
dbSNP: rs16879003
rs16879003
ATXN1
1.000 0.080 6 16745008 intron variant T/C;G snv
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery 		0.700 1.000 1 2017 2017
dbSNP: rs16879003
rs16879003
ATXN1
1.000 0.080 6 16745008 intron variant T/C;G snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.700 1.000 1 2017 2017
dbSNP: rs17603856
rs17603856
ATXN1
1.000 0.080 6 16630667 intron variant T/G snv 0.28
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 1.000 1 2016 2016
dbSNP: rs179992
rs179992
ATXN1
6 16324091 intron variant A/G snv 0.28
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs179994
rs179994
ATXN1
6 16320756 intron variant A/C snv 0.31
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs180001
rs180001
ATXN1
6 16315427 intron variant G/A;C snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs3819405
rs3819405
ATXN1
1.000 0.080 6 16399326 intron variant C/T snv 0.38
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.700 1.000 1 2017 2017
dbSNP: rs557966248
rs557966248
ATXN1
6 16322747 intron variant C/G;T snv
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs562760
rs562760
ATXN1
6 16749780 intron variant G/C;T snv 0.55
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2018 2018
dbSNP: rs6459480
rs6459480
ATXN1
1.000 0.040 6 16663232 intron variant G/A;C;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2019 2019
dbSNP: rs6459480
rs6459480
ATXN1
1.000 0.040 6 16663232 intron variant G/A;C;T snv
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs760882
rs760882
ATXN1
6 16658900 intron variant T/A snv 0.63
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs7770062
rs7770062
ATXN1
1.000 0.080 6 16413394 intron variant G/A snv 0.13
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.700 1.000 1 2018 2018
dbSNP: rs909788
rs909788
ATXN1
1.000 0.080 6 16636230 intron variant T/C snv 0.49
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 1.000 1 2017 2017