Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs620861
PCAT1 ; CASC8 ; POU5F1B ; CASC21
0.925 0.080 8 127323428 intron variant G/A snv 0.36 1
rs6486060
NRIP3 ; LOC105376541
11 9003083 intron variant G/A snv 0.55 1
rs6701231
TBX15
1 118953038 intron variant C/A;G snv 1
rs6784615
NISCH
1.000 0.080 3 52472410 intron variant C/T snv 0.96 0.96 1
rs6861681
CPEB4
5 173935455 intron variant G/A snv 0.22 1
rs6942652
CPED1
7 121249218 intron variant G/C;T snv 1
rs7246865
MYO9B
19 17108295 intron variant G/A snv 0.36 1
rs7637773
IGF2BP2
1.000 0.080 3 185797847 intron variant G/A snv 0.38 1
rs7745274
RSPO3 ; LOC112267972
6 127188012 intron variant G/A snv 0.56 1
rs7797307 7 69221140 intron variant G/C snv 7.6E-02 1
rs9302652
FTO
1.000 0.080 16 53832063 intron variant C/T snv 0.74 1
rs9491696
RSPO3
6 127131494 intron variant C/G snv 0.45 1
rs9515201
COL4A2
0.925 0.080 13 110388451 intron variant A/C snv 0.63 1
rs9647379
FNDC3B
3 172067378 intron variant G/C snv 0.32 1
rs984222
TBX15
1 118961220 intron variant C/A;G snv 1
rs987763
LOC105377989
6 126960402 intron variant C/A;T snv 1
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 6
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 3
rs12061508 1.000 0.040 1 196615338 intergenic variant G/A snv 0.23 2
rs12714415 2 651430 intergenic variant T/C snv 0.19 2
rs12110693
LOC105377979
6 121837124 intergenic variant G/A snv 0.23 1
rs17568628 5 76751114 intergenic variant T/C;G snv 1
rs2119690 8 20002028 intergenic variant G/A;C snv 1
rs2145272 20 6645571 intergenic variant G/A;T snv 1
rs2820464
LYPLAL1-AS1
1 219519878 intergenic variant G/A;C snv 1