SLC17A1, solute carrier family 17 member 1, 6568

N. diseases: 23; N. variants: 164
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: rs1183201
rs1183201
0.925 0.120 6 25823216 intron variant A/T snv 0.65
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.800 1.000 1 2009 2009
dbSNP: rs4712972
rs4712972
0.882 0.160 6 25771819 intron variant A/C;G snv
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
Cardiovascular Diseases 0.800 1.000 1 2011 2011
dbSNP: rs10498728
rs10498728
0.925 0.120 6 25751092 upstream gene variant T/A snv 0.21
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs10498730
rs10498730
0.925 0.120 6 25811841 intron variant A/G snv 3.7E-02
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 1 2013 2013
dbSNP: rs10498730
rs10498730
0.925 0.120 6 25811841 intron variant A/G snv 3.7E-02
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.700 1.000 1 2009 2009
dbSNP: rs10498730
rs10498730
0.925 0.120 6 25811841 intron variant A/G snv 3.7E-02
CUI: C0018099
Disease: Gout
Gout
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 1 2013 2013
dbSNP: rs10498730
rs10498730
0.925 0.120 6 25811841 intron variant A/G snv 3.7E-02
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs1141034
rs1141034
0.925 0.120 6 25780104 3 prime UTR variant C/T snv 0.26
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs1141034
rs1141034
0.925 0.120 6 25780104 3 prime UTR variant C/T snv 0.26
CUI: C0018099
Disease: Gout
Gout
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 1 2013 2013
dbSNP: rs1141034
rs1141034
0.925 0.120 6 25780104 3 prime UTR variant C/T snv 0.26
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 1 2013 2013
dbSNP: rs1165151
rs1165151
0.925 0.120 6 25821388 intron variant T/A;G snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs1165152
rs1165152
0.925 0.120 6 25818538 intron variant A/C;G;T snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs1165153
rs1165153
0.925 0.120 6 25817561 intron variant A/G;T snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs1165153
rs1165153
0.925 0.120 6 25817561 intron variant A/G;T snv
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.700 1.000 1 2009 2009
dbSNP: rs1165155
rs1165155
0.925 0.120 6 25795349 intron variant A/G;T snv
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 1 2013 2013
dbSNP: rs1165155
rs1165155
0.925 0.120 6 25795349 intron variant A/G;T snv
CUI: C0018099
Disease: Gout
Gout
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 1 2013 2013
dbSNP: rs1165156
rs1165156
0.925 0.120 6 25792750 intron variant T/C snv 0.38
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 1 2013 2013
dbSNP: rs1165156
rs1165156
0.925 0.120 6 25792750 intron variant T/C snv 0.38
CUI: C0018099
Disease: Gout
Gout
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 1 2013 2013
dbSNP: rs1165157
rs1165157
0.925 0.120 6 25792022 intron variant A/G snv 0.38
CUI: C0018099
Disease: Gout
Gout
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 1 2013 2013
dbSNP: rs1165157
rs1165157
0.925 0.120 6 25792022 intron variant A/G snv 0.38
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 1 2013 2013
dbSNP: rs1165176
rs1165176
0.925 0.120 6 25830070 intron variant A/G snv 0.65
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.700 1.000 1 2009 2009
dbSNP: rs1165176
rs1165176
0.925 0.120 6 25830070 intron variant A/G snv 0.65
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs1165177
rs1165177
0.925 0.120 6 25829431 intron variant T/A snv 0.65
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.700 1.000 1 2009 2009
dbSNP: rs1165177
rs1165177
0.925 0.120 6 25829431 intron variant T/A snv 0.65
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs1165178
rs1165178
0.925 0.120 6 25827288 intron variant A/G snv 0.65
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012