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: rs635634
rs635634 		0.882 0.160 9 133279427 upstream gene variant T/A;C snv
CUI: C2825910
Disease: Stem Cell Factor Measurement
Stem Cell Factor Measurement 		0.700 1.000 1 2017 2017
dbSNP: rs635634
rs635634 		0.882 0.160 9 133279427 upstream gene variant T/A;C snv
CUI: C0017741
Disease: Glucose tolerance test
Glucose tolerance test 		0.700 1.000 1 2017 2017
dbSNP: rs635634
rs635634 		0.882 0.160 9 133279427 upstream gene variant T/A;C snv
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2017 2017
dbSNP: rs635634
rs635634 		0.882 0.160 9 133279427 upstream gene variant T/A;C snv
CUI: C1531624
Disease: Cardioembolic stroke
Cardioembolic stroke 		0.700 1.000 1 2018 2018
dbSNP: rs635634
rs635634 		0.882 0.160 9 133279427 upstream gene variant T/A;C snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs635634
rs635634 		0.882 0.160 9 133279427 upstream gene variant T/A;C snv
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2017 2017
dbSNP: rs635634
rs635634 		0.882 0.160 9 133279427 upstream gene variant T/A;C snv
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs635634
rs635634 		0.882 0.160 9 133279427 upstream gene variant T/A;C snv
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs635634
rs635634 		0.882 0.160 9 133279427 upstream gene variant T/A;C snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs635634
rs635634 		0.882 0.160 9 133279427 upstream gene variant T/A;C snv
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.700 1.000 1 2018 2018
dbSNP: rs635634
rs635634 		0.882 0.160 9 133279427 upstream gene variant T/A;C snv
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		0.700 1.000 1 2016 2016
dbSNP: rs635634
rs635634 		0.882 0.160 9 133279427 upstream gene variant T/A;C snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs635634
rs635634 		0.882 0.160 9 133279427 upstream gene variant T/A;C snv
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement 		0.700 1.000 1 2019 2019
dbSNP: rs635634
rs635634 		0.882 0.160 9 133279427 upstream gene variant T/A;C snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.700 1.000 1 2017 2017
dbSNP: rs635634
rs635634 		0.882 0.160 9 133279427 upstream gene variant T/A;C snv
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.700 1.000 2 2017 2018
dbSNP: rs635634
rs635634 		0.882 0.160 9 133279427 upstream gene variant T/A;C snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 3 2010 2019
dbSNP: rs635634
rs635634 		0.882 0.160 9 133279427 upstream gene variant T/A;C snv
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.800 1.000 4 2010 2019