Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 11
rs17486278
CHRNA5
0.827 0.120 15 78575140 intron variant A/C snv 0.32 2
rs9268862
HLA-DRB9
0.925 0.160 6 32462390 intron variant A/C snv 0.29 2
rs10970384 1.000 0.040 9 3158247 intergenic variant A/C snv 0.21 1
rs11152369
TCF4
0.851 0.040 18 55399097 intron variant A/C snv 6.3E-02 1
rs13008971 1.000 0.040 2 8840342 upstream gene variant A/C snv 0.58 1
rs13025591
AGAP1
1.000 0.040 2 235886699 intron variant A/C snv 0.37 1
rs1345778
PTGER4 ; TTC33
1.000 0.040 5 40712695 3 prime UTR variant A/C snv 0.32 1
rs138880
BRD1
1.000 0.040 22 49824963 intron variant A/C snv 0.36 1
rs1530419
PPP2R2B
1.000 0.040 5 146648977 intron variant A/C snv 0.76 1
rs2239063
CACNA1C
1.000 0.040 12 2402665 intron variant A/C snv 0.23 1
rs3800316
POM121L2
1.000 0.040 6 27288323 intron variant A/C snv 0.33 1
rs4129585
TSNARE1 ; LOC107986983
1.000 0.040 8 142231572 intron variant A/C snv 0.68 1
rs4380187 0.925 0.040 2 184947213 intergenic variant A/C snv 0.34 1
rs7749823
H2BC5
1.000 0.040 6 26157851 upstream gene variant A/C snv 0.11 1
rs17693963 0.882 0.040 6 27742386 upstream gene variant A/C;G snv 3
rs1975802
PLA2G15
1.000 0.040 16 68251944 intron variant A/C;G snv 2
rs11038167
TSPAN18
1.000 0.040 11 44821583 intron variant A/C;G snv 1
rs12443954 0.851 0.040 16 89675088 intron variant A/C;G snv 1
rs420259
PALB2
0.925 0.040 16 23622705 intron variant A/C;G snv 1
rs5761163
MYO18B
1.000 0.040 22 25743411 intron variant A/C;G snv 1
rs9960767
TCF4
0.925 0.040 18 55487771 intron variant A/C;G snv 1
rs8091331 1.000 0.040 18 7392669 intergenic variant A/C;G;T snv 1
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs12991836
ZEB2
1.000 0.040 2 144383974 intron variant A/C;T snv 1