Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs999885
AP4M1 ; MCM7
0.925 0.120 7 100103553 intron variant G/A snv 0.56 0.46 1
rs9991479 4 28793250 intergenic variant T/C;G snv 1
rs9957921 18 60223839 intergenic variant G/A;C snv 1
rs9945304
NOL4
18 34123100 intron variant C/G;T snv 1
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18
rs988913
FAM83B
6 54891510 intron variant C/T snv 0.38 1
rs9849338 3 172408686 intergenic variant C/A;T snv 1
rs9849248 3 88192124 intergenic variant C/T snv 0.74 1
rs9795476
SIRT3 ; PSMD13
11 235894 intron variant T/G snv 0.79 1
rs9756797
SATB1 ; TBC1D5
3 18385985 intron variant G/A snv 0.33 1
rs9681954 3 86843214 intergenic variant T/A;C snv 1
rs9652589
PDILT
16 20359494 missense variant C/T snv 0.44 0.46 2
rs9647570
LOC105377709 ; TENM2
5 167943258 intron variant T/A;G snv 1
rs9640621 7 94464841 intergenic variant C/T snv 0.67 1
rs9635759 17 51536424 regulatory region variant G/A snv 0.25 2
rs9616551 22 49284503 intergenic variant A/C;G snv 1
rs9603605
COG6
13 39734170 intron variant T/C snv 0.29 1
rs9568125 13 48902179 regulatory region variant C/T snv 0.16 1
rs9560114 13 111535535 intergenic variant A/T snv 0.21 1
rs9560113 13 111531001 regulatory region variant A/G snv 0.26 1
rs9555810 13 111529090 intergenic variant C/G;T snv 1
rs9554311
PAN3
13 28293131 3 prime UTR variant C/T snv 0.56 1
rs9517913
LOC101927437
13 99912254 intron variant G/A snv 0.30 1
rs951366
NUCKS1
0.925 0.240 1 205716224 3 prime UTR variant T/C snv 0.34 3
rs9475752
DST
6 56915943 intron variant C/T snv 0.23 1