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: rs6855911
rs6855911
SLC2A9
4 0.851 0.200 4 9934286 intron variant A/G snv 0.33 0.700 1.000 4 2007 2013
dbSNP: rs7442295
rs7442295
SLC2A9
4 0.925 0.120 4 9964756 intron variant A/G snv 0.28 0.700 1.000 5 2008 2013
dbSNP: rs16890979
rs16890979
SLC2A9
4 0.827 0.200 4 9920543 missense variant C/T snv 0.24 0.29 0.710 1.000 4 2008 2016
dbSNP: rs2231142
rs2231142
ABCG2
3 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 0.820 1.000 4 2008 2019
dbSNP: rs737267
rs737267
SLC2A9
4 0.851 0.240 4 9933120 intron variant G/A;T snv 0.700 1.000 4 2008 2013
dbSNP: rs1165205
rs1165205
SLC17A3
4 0.925 0.120 6 25870314 intron variant T/A;G snv 0.700 1.000 3 2008 2013
dbSNP: rs10001106
rs10001106 		3 0.925 0.120 4 10125817 intergenic variant T/A;C snv 0.700 1.000 3 2010 2013
dbSNP: rs10003001
rs10003001
SLC2A9
3 0.925 0.120 4 9982851 intron variant C/T snv 0.21 0.700 1.000 3 2010 2013
dbSNP: rs10006397
rs10006397
SLC2A9
3 0.925 0.120 4 10034516 non coding transcript exon variant C/A snv 0.78 0.700 1.000 3 2010 2013
dbSNP: rs10009618
rs10009618
ABCG2
3 0.925 0.120 4 88172856 intron variant C/T snv 0.58 0.700 1.000 3 2010 2013
dbSNP: rs10011796
rs10011796
ABCG2
3 0.882 0.160 4 88169725 intron variant T/C;G snv 0.800 1.000 3 2010 2015
dbSNP: rs10022499
rs10022499
SLC2A9 ; LOC105374476
3 0.925 0.120 4 10004913 intron variant C/A snv 0.72 0.700 1.000 3 2010 2013
dbSNP: rs10023068
rs10023068
SLC2A9 ; LOC105374476
3 0.925 0.120 4 10003208 intron variant A/G snv 0.72 0.700 1.000 3 2010 2013
dbSNP: rs10033612
rs10033612
SLC2A9
3 0.925 0.120 4 9983382 intron variant C/T snv 0.20 0.700 1.000 3 2010 2013
dbSNP: rs1014290
rs1014290
SLC2A9 ; LOC105374476
3 0.827 0.280 4 10000237 intron variant G/A snv 0.72 0.810 1.000 3 2010 2019
dbSNP: rs10516200
rs10516200
WDR1 ; MIR3138
3 0.925 0.120 4 10080532 intron variant C/A;T snv 0.700 1.000 3 2010 2013
dbSNP: rs10516201
rs10516201 		3 0.925 0.120 4 10122317 intergenic variant T/C snv 0.18 0.700 1.000 3 2010 2013
dbSNP: rs1071988
rs1071988
SLC2A9
3 0.925 0.120 4 9973014 intron variant A/G;T snv 0.700 1.000 3 2010 2013
dbSNP: rs1079128
rs1079128
SLC2A9
3 0.925 0.120 4 9949597 intron variant T/C snv 0.51 0.700 1.000 3 2010 2013
dbSNP: rs10792443
rs10792443
NRXN2
2 0.925 0.120 11 64627780 intron variant G/C snv 0.51 0.700 1.000 3 2010 2013
dbSNP: rs10805346
rs10805346
SLC2A9
3 0.925 0.120 4 9918723 intron variant T/C snv 0.51 0.700 1.000 3 2010 2013
dbSNP: rs10897526
rs10897526
MAP4K2
2 0.925 0.120 11 64792426 splice region variant T/C snv 0.37 0.30 0.700 1.000 3 2010 2013
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 3 2010 2013
dbSNP: rs10939665
rs10939665
SLC2A9
3 0.925 0.120 4 10036004 non coding transcript exon variant T/C snv 0.43 0.700 1.000 3 2010 2013
dbSNP: rs10939669
rs10939669
SLC2A9
3 0.925 0.120 4 10044203 intron variant A/G;T snv 0.700 1.000 3 2010 2013