Source: GWASDB

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: rs12029454
rs12029454
1 162163327 intron variant G/A snv 0.21
QT interval feature (observable entity)
0.800 1.000 2 2009 2019
dbSNP: rs4657175
rs4657175
1.000 0.040 1 162225948 intron variant T/C;G snv
QT interval feature (observable entity)
0.800 1.000 2 2012 2019
dbSNP: rs10494366
rs10494366
0.851 0.200 1 162115895 intron variant G/T snv 0.54
QT interval feature (observable entity)
0.800 1.000 1 2006 2019
dbSNP: rs16857031
rs16857031
1 162143120 intron variant C/G snv 0.18
QT interval feature (observable entity)
0.800 1.000 1 2009 2019
dbSNP: rs3934467
rs3934467
1 162212887 intron variant C/T snv 0.27
QT interval feature (observable entity)
0.800 1.000 1 2012 2019
dbSNP: rs4657178
rs4657178
1 162240820 intron variant C/A;G;T snv 0.31
QT interval feature (observable entity)
0.800 1.000 1 2009 2019
dbSNP: rs10127719
rs10127719
1 162186380 intron variant T/A;C snv
QT interval feature (observable entity)
0.700 1.000 1 2012 2012
dbSNP: rs10800352
rs10800352
1 162202899 intron variant A/G snv 0.27
QT interval feature (observable entity)
0.700 1.000 1 2012 2012
dbSNP: rs10918602
rs10918602
1 162067910 upstream gene variant T/C snv 0.25
QT interval feature (observable entity)
0.700 1.000 1 2012 2012
dbSNP: rs10918796
rs10918796
1 162163553 intron variant C/A;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2011 2011
dbSNP: rs10919021
rs10919021
1 162265600 intron variant C/T snv 0.97
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs11805598
rs11805598
1 162170546 intron variant A/G snv 0.44
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2011 2011
dbSNP: rs12027785
rs12027785
1 162211355 intron variant T/A snv 0.27
QT interval feature (observable entity)
0.700 1.000 1 2012 2012
dbSNP: rs12116744
rs12116744
1 162210666 intron variant G/A snv 0.27
QT interval feature (observable entity)
0.700 1.000 1 2012 2012
dbSNP: rs12123267
rs12123267
1 162229561 intron variant C/T snv 0.27
QT interval feature (observable entity)
0.700 1.000 1 2012 2012
dbSNP: rs12135795
rs12135795
1 162179975 intron variant A/G snv 0.44
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2011 2011
dbSNP: rs12567315
rs12567315
1 162196856 intron variant G/A snv 0.27
QT interval feature (observable entity)
0.700 1.000 1 2012 2012
dbSNP: rs12724220
rs12724220
1 162183208 intron variant A/G snv 0.44
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2011 2011
dbSNP: rs12734991
rs12734991
1 162224786 intron variant C/T snv 0.41
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2011 2011
dbSNP: rs1337068
rs1337068
1 162163356 intron variant G/A snv 0.96
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs1510291
rs1510291
1 162358271 intron variant C/T snv 3.5E-02
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs1510291
rs1510291
1 162358271 intron variant C/T snv 3.5E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs16860953
rs16860953
1 162364127 5 prime UTR variant G/A snv 2.1E-02
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs16860953
rs16860953
1 162364127 5 prime UTR variant G/A snv 2.1E-02
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs1912439
rs1912439
1 162324355 intron variant A/G snv 0.98
High density lipoprotein measurement
0.700 1.000 1 2012 2012