rs760077, MTX1;THBS3

N. diseases: 8
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Blood urea nitrogen measurement
CUI: C0005845
Disease: Blood urea nitrogen measurement
174 0.925 0.120 1 155208991 missense variant T/A snv 0.36 0.700 1.000 2 2017 2019
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 0.925 0.120 1 155208991 missense variant T/A snv 0.36 0.700 1.000 2 2016 2019
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.925 0.120 1 155208991 missense variant T/A snv 0.36 0.700 1.000 2 2015 2020
Glomerular Filtration Rate
CUI: C0017654
Disease: Glomerular Filtration Rate
1033 0.925 0.120 1 155208991 missense variant T/A snv 0.36 0.700 1.000 1 2019 2019
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
216 0.925 0.120 1 155208991 missense variant T/A snv 0.36 0.700 1.000 1 2016 2016
Hemoglobin measurement
CUI: C0518015
Disease: Hemoglobin measurement
224 0.925 0.120 1 155208991 missense variant T/A snv 0.36 0.700 1.000 1 2016 2016
Uric acid measurement (procedure)
CUI: C0202239
Disease: Uric acid measurement (procedure)
1463 0.925 0.120 1 155208991 missense variant T/A snv 0.36 0.700 1.000 1 2019 2019
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.925 0.120 1 155208991 missense variant T/A snv 0.36 0.010 1.000 1 2011 2011