Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs603424
PKD2L1
1.000 0.080 10 100315722 intron variant G/A snv 0.34 4
rs2569512
ILF3
0.925 0.080 19 10679486 intron variant T/C snv 0.76 1
rs1933182 1.000 0.080 1 109457216 intergenic variant A/C snv 0.63 1
rs4773144
COL4A1 ; COL4A2
0.827 0.080 13 110308365 intron variant A/G snv 0.42 3
rs10794720
WDR37
1.000 0.080 10 1110225 intron variant T/C snv 0.89 1
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 7
rs7901695
TCF7L2
0.851 0.160 10 112994329 intron variant T/C snv 0.34 2
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs6046
F7
0.925 0.080 13 113118845 missense variant G/A;C;T snv 0.13 1
rs2266788
APOA5 ; ZPR1
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 7
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 6
rs10068737 5 118700852 intergenic variant T/A;C snv 1
rs2014355
ACADS
0.925 0.120 12 120737721 non coding transcript exon variant T/C snv 0.22 1
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 1
rs1009840
SGK1 ; LOC107986646
6 134225547 intron variant G/A snv 0.53 1
rs12575381 11 135033566 regulatory region variant G/A snv 0.16 1
rs347685
TFDP2
1.000 0.080 3 142088295 intron variant C/A snv 0.74 1
rs267734 0.925 0.120 1 150979001 upstream gene variant T/C snv 0.14 1
rs7805747
PRKAG2
1.000 0.080 7 151710715 intron variant G/A snv 0.26 2
rs4845625
IL6R
0.851 0.080 1 154449591 intron variant T/C snv 0.60 3
rs12124078
DNAJC16
1 15543404 intron variant A/G snv 0.32 1
rs6431731
LINC01804
1.000 0.080 2 15722878 intron variant C/T snv 0.97 1
rs2880072 6 159404417 downstream gene variant G/A snv 0.49 1
rs3093058
CRP
1 159715525 upstream gene variant T/A;C;G snv 1