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: rs1165152
rs1165152
6 25818538 intron variant A/C,G,T snp 0.67
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.800 4 2009 2016
dbSNP: rs1165196
rs1165196
6 25812922 missense variant G/A snp 0.62 0.67
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.800 4 2009 2016
dbSNP: rs1165209
rs1165209
6 25801091 intron variant G/A snp 0.67
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.800 4 2009 2016
dbSNP: rs11754288
rs11754288
6 25776721 missense variant G/A snp 0.36 0.31
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.800 4 2009 2013
dbSNP: rs1165151
rs1165151
6 25821388 intron variant T/A,G snp 6.4E-05; 0.66
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.800 3 2009 2013
dbSNP: rs1183201
rs1183201
6 25823216 intron variant A/T snp 0.66
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.800 3 2009 2013
dbSNP: rs17342717
rs17342717
6 25821542 intron variant C/T snp 6.5E-02
Erythrocyte Mean Corpuscular Hemoglobin Test
0.800 3 2011 2012
dbSNP: rs17342717
rs17342717
6 25821542 intron variant C/T snp 6.5E-02
Finding of Mean Corpuscular Hemoglobin
0.800 3 2011 2012
dbSNP: rs17342717
rs17342717
6 25821542 intron variant C/T snp 6.5E-02
CUI: C0373607
Disease: Ferritin measurement
Ferritin measurement
0.800 2 2011 2011
dbSNP: rs4712972
rs4712972
1.000 0.036 6 25771819 intron variant A/C,G snp 3.2E-05; 0.78
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
Cardiovascular Diseases 0.800 1 2011 2011
dbSNP: rs13200784
rs13200784
6 25829405 intron variant A/T snp 0.27
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.700 4 2009 2013
dbSNP: rs1408268
rs1408268
6 25826758 intron variant T/A snp 0.27
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.700 4 2009 2013
dbSNP: rs6456703
rs6456703
6 25825891 intron variant C/T snp 0.26
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.700 4 2009 2013
dbSNP: rs1165153
rs1165153
6 25817561 intron variant A/G,T snp 0.67
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.700 3 2009 2013
dbSNP: rs1165176
rs1165176
1.000 0.107 6 25830070 intron variant A/G snp 0.66
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.700 3 2009 2013
dbSNP: rs1165177
rs1165177
6 25829431 intron variant T/A snp 0.66
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.700 3 2009 2013
dbSNP: rs1165178
rs1165178
6 25827288 intron variant A/G snp 0.66
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.700 3 2009 2013
dbSNP: rs1165215
rs1165215
6 25798704 3 prime UTR variant G/A snp 0.67
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.700 3 2009 2013
dbSNP: rs1183200
rs1183200
6 25818418 intron variant G/C snp 0.67
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.700 3 2009 2013
dbSNP: rs1185567
rs1185567
6 25818360 intron variant A/G,T snp 0.67
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.700 3 2009 2013
dbSNP: rs1185569
rs1185569
6 25831375 intron variant A/G snp 0.66
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.700 3 2009 2013
dbSNP: rs13197601
rs13197601
6 25785707 intron variant G/A snp 0.30
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.700 3 2009 2013
dbSNP: rs1324082
rs1324082
6 25801743 intron variant C/T snp 0.28
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.700 3 2009 2013
dbSNP: rs2762353
rs2762353
6 25794203 intron variant A/G snp 0.67
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.700 3 2009 2013
dbSNP: rs3757131
rs3757131
6 25783681 intron variant C/T snp 0.31
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.700 3 2009 2013