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: rs1165151
rs1165151
SLC17A1
4 0.925 0.120 6 25821388 intron variant T/A;G snv 0.800 1.000 2 2009 2013
dbSNP: rs1165152
rs1165152
SLC17A1
4 0.925 0.120 6 25818538 intron variant A/C;G;T snv 0.800 1.000 2 2009 2015
dbSNP: rs1165178
rs1165178
SLC17A1
4 0.925 0.120 6 25827288 intron variant A/G snv 0.65 0.800 1.000 2 2009 2019
dbSNP: rs1165205
rs1165205
SLC17A3
4 0.925 0.120 6 25870314 intron variant T/A;G snv 0.800 1.000 2 2008 2009
dbSNP: rs1165209
rs1165209
SLC17A1
4 0.925 0.120 6 25801091 intron variant G/A snv 0.66 0.800 1.000 2 2009 2015
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 2 2009 2011
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: rs12504795
rs12504795
CLNK ; LOC105374482
3 0.925 0.120 4 10497720 intron variant T/C snv 0.23 0.800 1.000 2 2009 2019
dbSNP: rs2728099
rs2728099
PKD2
3 0.925 0.120 4 88054586 intron variant T/C snv 8.0E-02 0.800 1.000 2 2009 2017
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: 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: rs4698036
rs4698036 		4 0.925 0.120 4 10329670 intergenic variant T/G snv 0.21 0.800 1.000 2 2009 2011
dbSNP: rs504915
rs504915
NRXN2
3 0.925 0.120 11 64696613 intron variant T/A;C snv 0.800 1.000 2 2012 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: rs780093
rs780093
GCKR
30 0.763 0.240 2 27519736 intron variant T/C snv 0.68 0.800 1.000 2 2009 2010
dbSNP: rs780094
rs780094
GCKR
62 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.800 1.000 2 2009 2015
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: rs17300741
rs17300741
SLC22A11
3 0.925 0.120 11 64563990 intron variant A/G;T snv 0.800 1.000 1 2009 2009