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: 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: 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: rs164009
rs164009
QRICH2
3 0.925 0.120 17 76287588 intron variant A/G snv 0.53 0.700 1.000 2 2013 2019
dbSNP: rs16856823
rs16856823
LRP2
3 2 169343942 intron variant A/T snv 4.6E-02 0.700 1.000 2 2018 2019
dbSNP: rs17632159
rs17632159
LOC105379030
3 0.925 0.120 5 73135655 intron variant G/A;C snv 0.700 1.000 2 2013 2019
dbSNP: rs2075251
rs2075251
LRP2
1 2 169154948 intron variant T/A;C snv 0.700 1.000 2 2018 2019
dbSNP: rs2220970
rs2220970
SBF2
1 11 9836202 intron variant G/A snv 0.80 0.700 1.000 2 2018 2019
dbSNP: rs2244608
rs2244608
HNF1A ; HNF1A-AS1
9 0.882 0.160 12 120979185 intron variant A/G snv 0.29 0.700 1.000 2 2013 2019
dbSNP: rs2390793
rs2390793
LRP2
1 2 169348613 intron variant C/A;T snv 0.700 1.000 2 2019 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: 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: rs504915
rs504915
NRXN2
3 0.925 0.120 11 64696613 intron variant T/A;C snv 0.800 1.000 2 2012 2018
dbSNP: rs57633992
rs57633992
NRXN2 ; NRXN2-AS1
1 11 64657495 intron variant C/A;T snv 0.700 1.000 2 2018 2019
dbSNP: rs6031598
rs6031598
HNF4A
1 20 44427509 intron variant G/A;T snv 0.700 1.000 2 2019 2019
dbSNP: rs626277
rs626277
DACH1
5 1.000 0.080 13 71773564 intron variant A/C snv 0.51 0.700 1.000 2 2019 2019
dbSNP: rs642803
rs642803
OVOL1
4 0.925 0.120 11 65793149 intron variant C/T snv 0.42 0.700 1.000 2 2013 2019
dbSNP: rs6445559
rs6445559 		1 3 53065450 intron variant A/G;T snv 0.700 1.000 2 2018 2019
dbSNP: rs6770152
rs6770152 		3 0.925 0.120 3 53066198 intron variant G/T snv 0.61 0.700 1.000 2 2013 2019
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: rs7224610
rs7224610
HLF
4 0.925 0.120 17 55287427 intron variant C/A;G snv 0.700 1.000 2 2013 2019
dbSNP: rs734553
rs734553
SLC2A9
7 0.851 0.240 4 9921380 intron variant G/A;T snv 0.800 1.000 2 2009 2011