Gene: SLC2A9 ×
Source: ALL
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: rs3775948
rs3775948
SLC2A9 ; LOC105374476
4 0.882 0.160 4 9993558 intron variant G/A;C snv 0.800 1.000 8 2009 2019
dbSNP: rs13129697
rs13129697
SLC2A9
5 0.925 0.120 4 9925343 intron variant T/G snv 0.39 0.800 1.000 6 2009 2018
dbSNP: rs16890979
rs16890979
SLC2A9
7 0.827 0.200 4 9920543 missense variant C/T snv 0.24 0.29 0.800 1.000 5 2008 2016
dbSNP: rs11722228
rs11722228
SLC2A9
6 0.851 0.160 4 9914117 intron variant C/T snv 0.32 0.800 1.000 4 2009 2019
dbSNP: rs6449213
rs6449213
SLC2A9 ; LOC105374476
7 0.827 0.240 4 9992591 intron variant C/T snv 0.82 0.800 1.000 4 2009 2017
dbSNP: rs13111638
rs13111638
SLC2A9 ; LOC105374476
4 0.882 0.200 4 9995266 intron variant T/C snv 0.82 0.800 1.000 3 2009 2018
dbSNP: rs737267
rs737267
SLC2A9
7 0.851 0.240 4 9933120 intron variant G/A;T snv 0.800 1.000 3 2008 2016
dbSNP: rs7442295
rs7442295
SLC2A9
5 0.925 0.120 4 9964756 intron variant A/G snv 0.28 0.800 1.000 3 2008 2009
dbSNP: rs10805346
rs10805346
SLC2A9
3 0.925 0.120 4 9918723 intron variant T/C snv 0.51 0.800 1.000 2 2009 2015
dbSNP: rs12498742
rs12498742
SLC2A9
3 0.925 0.120 4 9942428 intron variant A/G snv 0.33 0.800 1.000 2 2009 2013
dbSNP: rs4385059
rs4385059
SLC2A9 ; LOC105374476
3 0.925 0.120 4 9987609 intron variant C/T snv 0.84 0.800 1.000 2 2009 2018
dbSNP: rs6832439
rs6832439
SLC2A9
3 0.925 0.120 4 9922695 intron variant A/G snv 0.70 0.800 1.000 2 2009 2013
dbSNP: rs6855911
rs6855911
SLC2A9
7 0.851 0.200 4 9934286 intron variant A/G snv 0.33 0.800 1.000 2 2007 2009
dbSNP: rs734553
rs734553
SLC2A9
7 0.851 0.240 4 9921380 intron variant G/A;T snv 0.800 1.000 2 2009 2011
dbSNP: rs7671266
rs7671266
SLC2A9
4 0.925 0.120 4 10054752 intron variant T/C snv 0.73 0.800 1.000 2 2009 2011
dbSNP: rs7675964
rs7675964
SLC2A9
3 0.925 0.120 4 9939810 intron variant C/T snv 0.39 0.800 1.000 2 2009 2019
dbSNP: rs7680126
rs7680126
SLC2A9
3 0.925 0.120 4 9983972 intron variant G/A snv 0.80 0.800 1.000 2 2009 2015
dbSNP: rs7679724
rs7679724
SLC2A9
1 4 9983752 intron variant G/T snv 0.65 0.700 1.000 3 2018 2019
dbSNP: rs10939650
rs10939650
SLC2A9 ; LOC105374476
3 0.925 0.120 4 9996816 synonymous variant C/G;T snv 1.2E-05; 0.70 0.700 1.000 2 2009 2011
dbSNP: rs13113918
rs13113918
SLC2A9 ; LOC105374476
3 0.925 0.120 4 9996869 synonymous variant A/G snv 0.80 0.79 0.700 1.000 2 2009 2011
dbSNP: rs3733588
rs3733588
SLC2A9 ; LOC105374476
3 0.925 0.120 4 9995679 non coding transcript exon variant G/A snv 0.72 0.700 1.000 2 2009 2011
dbSNP: rs4529048
rs4529048
SLC2A9 ; LOC105374476
3 0.925 0.120 4 9995488 intron variant C/A;T snv 0.700 1.000 2 2009 2011
dbSNP: rs7663032
rs7663032
SLC2A9 ; LOC105374476
3 0.925 0.120 4 9992214 intron variant C/G;T snv 0.71 0.700 1.000 2 2009 2011
dbSNP: rs10001964
rs10001964
SLC2A9
3 0.925 0.120 4 9957651 intron variant C/T snv 0.48 0.700 1.000 1 2009 2009
dbSNP: rs10003001
rs10003001
SLC2A9
3 0.925 0.120 4 9982851 intron variant C/T snv 0.21 0.700 1.000 1 2009 2009