Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 8
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 6
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 6
rs3131296
NOTCH4
0.807 0.320 6 32205216 intron variant C/T snv 0.11 6
rs7762279 0.807 0.360 6 32787513 intergenic variant T/C snv 8.4E-02 6
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 5
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 5
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 4
rs13211507
PGBD1
0.882 0.200 6 28289600 intron variant T/C snv 6.4E-02 4
rs1480380
HLA-DMB
0.763 0.360 6 32945469 intron variant C/T snv 0.11 4
rs389883
CYP21A2 ; STK19
0.827 0.200 6 31979683 non coding transcript exon variant G/T snv 0.80 4
rs4537545
IL6R
0.790 0.160 1 154446403 intron variant C/T snv 0.48 4
rs8042374
CHRNA3
0.807 0.200 15 78615690 intron variant A/G snv 0.29 4
rs8283
ATF6B ; TNXB
0.882 0.120 6 32115523 3 prime UTR variant A/G snv 0.25 4
rs9268856
HLA-DRB9
0.807 0.240 6 32461942 intron variant C/A;T snv 4
rs9272219
HLA-DQA1
0.925 0.160 6 32634492 intron variant G/T snv 0.29 4
rs9467626
SLC17A3
0.882 0.160 6 25873518 intron variant C/A snv 7.3E-02 4
rs10275045
MAD1L1
0.882 0.160 7 1881190 intron variant C/T snv 0.35 3
rs10484399 0.851 0.240 6 27566749 intergenic variant A/G snv 5.4E-02 3
rs10994359
ANK3
0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 3
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 3
rs12061601 1.000 0.040 1 169101212 intron variant T/C snv 0.16 3
rs13199775
SLC17A1
0.882 0.160 6 25828554 intron variant A/T snv 7.4E-02 3