Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10790519
rs10790519 		11 122664700 intron variant T/C snv 0.39
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs10892873
rs10892873 		11 122664625 intron variant G/C;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs1106243
rs1106243 		11 122740722 intron variant G/A;C snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs1945397
rs1945397 		11 122727894 intron variant A/G snv 0.32
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs35483388
rs35483388 		11 122674438 intron variant C/T snv 0.39
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs4427576
rs4427576 		11 122739171 intron variant A/T snv 0.33
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs7115089
rs7115089 		11 122659883 intron variant C/G snv 0.39
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs7117842
rs7117842 		11 122663796 intron variant T/C snv 0.38
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2017 2017
dbSNP: rs7128198
rs7128198 		11 122655893 5 prime UTR variant C/G;T snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs7128198
rs7128198 		11 122655893 5 prime UTR variant C/G;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2015 2015
dbSNP: rs7129204
rs7129204 		11 122656504 intron variant G/C snv 0.15
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.700 1.000 1 2019 2019
dbSNP: rs7936300
rs7936300 		11 122730326 intron variant A/G snv 0.34
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement 		0.700 1.000 1 2019 2019
dbSNP: rs4936742
rs4936742 		0.925 0.200 11 122770378 intron variant T/C snv 0.64
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Cardiovascular Diseases 0.010 1.000 1 2019 2019
dbSNP: rs4936742
rs4936742 		0.925 0.200 11 122770378 intron variant T/C snv 0.64
CUI: C0042167
Disease: Uveitis, Posterior
Uveitis, Posterior 		Eye Diseases 0.010 1.000 1 2019 2019