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: rs10939679
rs10939679
SLC2A9
2 0.925 0.120 4 10054231 intron variant T/C snv 0.13 0.700 1.000 1 2011 2011
dbSNP: rs10939681
rs10939681
SLC2A9
2 0.925 0.120 4 10054340 intron variant A/C snv 0.13 0.700 1.000 1 2011 2011
dbSNP: rs12499734
rs12499734
SLC2A9
2 0.925 0.120 4 10050137 intron variant C/T snv 9.9E-02 0.700 1.000 1 2011 2011
dbSNP: rs12642537
rs12642537
SLC2A9
2 0.925 0.120 4 10035997 non coding transcript exon variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs12800450
rs12800450
SLC22A12
3 0.925 0.120 11 64591749 missense variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs13106922
rs13106922
SLC2A9
2 0.925 0.120 4 10020135 intron variant A/G snv 9.9E-02 0.700 1.000 1 2011 2011
dbSNP: rs13122112
rs13122112
SLC2A9
2 0.925 0.120 4 10019780 intron variant G/A snv 9.9E-02 0.700 1.000 1 2011 2011
dbSNP: rs13135351
rs13135351
SLC2A9
2 0.925 0.120 4 10031901 intron variant G/A snv 8.6E-02 0.700 1.000 1 2011 2011
dbSNP: rs16892475
rs16892475
SLC2A9
2 0.925 0.120 4 10038649 intron variant A/C snv 1.0E-01 0.700 1.000 1 2011 2011
dbSNP: rs16892493
rs16892493
SLC2A9
2 0.925 0.120 4 10040023 intron variant C/T snv 9.5E-02 0.700 1.000 1 2011 2011
dbSNP: rs198806
rs198806
H2AC6
4 0.925 0.120 6 26133388 intron variant A/G snv 0.59 0.700 1.000 1 2011 2011
dbSNP: rs3756231
rs3756231
SLC2A9
2 0.925 0.120 4 10023920 intron variant A/G snv 7.3E-02 0.700 1.000 1 2011 2011
dbSNP: rs3775939
rs3775939
SLC2A9
2 0.925 0.120 4 10023672 intron variant C/G snv 9.9E-02 0.700 1.000 1 2011 2011
dbSNP: rs3775941
rs3775941
SLC2A9
2 0.925 0.120 4 10023469 intron variant T/A snv 9.9E-02 0.700 1.000 1 2011 2011
dbSNP: rs3796840
rs3796840
SLC2A9 ; LOC105374476
2 0.925 0.120 4 10006497 non coding transcript exon variant C/T snv 6.1E-02 0.700 1.000 1 2011 2011
dbSNP: rs493573
rs493573
MAP4K2
3 0.925 0.120 11 64789582 synonymous variant C/T snv 1.6E-03 6.8E-03 0.700 1.000 1 2011 2011
dbSNP: rs589691
rs589691
PYGM
3 0.925 0.120 11 64757744 intron variant C/T snv 4.0E-06; 0.79 0.69 0.700 1.000 1 2011 2011
dbSNP: rs606458
rs606458
SF1
4 0.882 0.160 11 64778919 upstream gene variant C/A;T snv 0.71 0.700 1.000 1 2011 2011
dbSNP: rs6821843
rs6821843
SLC2A9
2 0.925 0.120 4 10050904 intron variant C/A snv 0.10 0.700 1.000 1 2011 2011
dbSNP: rs7683832
rs7683832
SLC2A9
2 0.925 0.120 4 10054458 intron variant G/A snv 0.13 0.700 1.000 1 2011 2011
dbSNP: rs9321453
rs9321453
LINC01010 ; CT69
3 0.925 0.120 6 134452416 intron variant T/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs10225163
rs10225163
JAZF1
2 0.925 0.120 7 27886026 intron variant C/G snv 0.53 0.700 1.000 1 2012 2012
dbSNP: rs10239506
rs10239506
PDE1C
2 0.925 0.120 7 32177281 intron variant C/G snv 0.57 0.700 1.000 1 2012 2012
dbSNP: rs10769025
rs10769025
ALX4
3 0.882 0.160 11 44267885 intron variant G/C snv 0.58 0.700 1.000 1 2012 2012
dbSNP: rs10773971
rs10773971
WNT5B
2 0.925 0.120 12 1631005 5 prime UTR variant C/G snv 6.8E-02 0.700 1.000 1 2012 2012