Source: GWASDB ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs13129697
rs13129697
SLC2A9
4 0.925 0.120 4 9925343 intron variant T/G snv 0.39 0.800 1.000 3 2009 2018
dbSNP: rs3775948
rs3775948
SLC2A9 ; LOC105374476
3 0.882 0.160 4 9993558 intron variant G/A;C snv 0.800 1.000 3 2009 2019
dbSNP: rs6449213
rs6449213
SLC2A9 ; LOC105374476
3 0.827 0.240 4 9992591 intron variant C/T snv 0.82 0.800 1.000 3 2009 2017
dbSNP: rs13111638
rs13111638
SLC2A9 ; LOC105374476
3 0.882 0.200 4 9995266 intron variant T/C snv 0.82 0.800 1.000 2 2009 2018
dbSNP: rs16890979
rs16890979
SLC2A9
4 0.827 0.200 4 9920543 missense variant C/T snv 0.24 0.29 0.800 1.000 2 2008 2016
dbSNP: rs4698014
rs4698014 		3 0.925 0.120 4 10284677 downstream gene variant C/T snv 0.18 0.800 1.000 2 2009 2013
dbSNP: rs10011796
rs10011796
ABCG2
3 0.882 0.160 4 88169725 intron variant T/C;G snv 0.800 1.000 1 2009 2015
dbSNP: rs10017305
rs10017305 		3 0.925 0.120 4 10399599 intergenic variant T/C snv 0.26 0.800 1.000 1 2009 2019
dbSNP: rs10805346
rs10805346
SLC2A9
3 0.925 0.120 4 9918723 intron variant T/C snv 0.51 0.800 1.000 1 2009 2015
dbSNP: rs10897518
rs10897518
SLC22A12
3 0.925 0.120 11 64593233 intron variant C/T snv 0.51 0.800 1.000 1 2009 2015
dbSNP: rs10910845
rs10910845 		3 0.925 0.120 1 145711946 upstream gene variant T/G snv 0.44 0.800 1.000 1 2009 2019
dbSNP: rs1165151
rs1165151
SLC17A1
4 0.925 0.120 6 25821388 intron variant T/A;G snv 0.800 1.000 1 2009 2013
dbSNP: rs1165152
rs1165152
SLC17A1
4 0.925 0.120 6 25818538 intron variant A/C;G;T snv 0.800 1.000 1 2009 2015
dbSNP: rs1165178
rs1165178
SLC17A1
4 0.925 0.120 6 25827288 intron variant A/G snv 0.65 0.800 1.000 1 2009 2019
dbSNP: rs1165196
rs1165196
SLC17A1
4 0.882 0.200 6 25812922 missense variant G/A snv 0.62 0.66 0.800 1.000 1 2009 2018
dbSNP: rs1165205
rs1165205
SLC17A3
4 0.925 0.120 6 25870314 intron variant T/A;G snv 0.800 1.000 1 2008 2009
dbSNP: rs1165209
rs1165209
SLC17A1
4 0.925 0.120 6 25801091 intron variant G/A snv 0.66 0.800 1.000 1 2009 2015
dbSNP: rs11722228
rs11722228
SLC2A9
4 0.851 0.160 4 9914117 intron variant C/T snv 0.32 0.800 1.000 1 2009 2019
dbSNP: rs11754288
rs11754288
SLC17A1 ; SLC17A4
4 0.925 0.120 6 25776721 missense variant G/A snv 0.36 0.32 0.800 1.000 1 2009 2011
dbSNP: rs1183201
rs1183201
SLC17A1
4 0.925 0.120 6 25823216 intron variant A/T snv 0.65 0.800 1.000 1 2009 2009
dbSNP: rs12129861
rs12129861
PDZK1
3 0.925 0.120 1 145709377 upstream gene variant C/T snv 0.43 0.800 1.000 1 2009 2009
dbSNP: rs12356193
rs12356193
SLC16A9
3 0.925 0.120 10 59653595 intron variant A/G snv 0.12 0.800 1.000 1 2009 2009
dbSNP: rs12498742
rs12498742
SLC2A9
3 0.925 0.120 4 9942428 intron variant A/G snv 0.33 0.800 1.000 1 2009 2013
dbSNP: rs12504795
rs12504795
CLNK ; LOC105374482
3 0.925 0.120 4 10497720 intron variant T/C snv 0.23 0.800 1.000 1 2009 2019
dbSNP: rs1260326
rs1260326
GCKR
25 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.800 1.000 1 2009 2019