Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 5
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 4
rs10994359
ANK3
0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 3
rs12061601 1.000 0.040 1 169101212 intron variant T/C snv 0.16 3
rs17693963 0.882 0.040 6 27742386 upstream gene variant A/C;G snv 3
rs2070016
FGA
1.000 0.040 4 154589162 intron variant A/G snv 0.12 3
rs253
LPL
1.000 0.040 8 19953906 intron variant C/T snv 0.53 3
rs4356203
PIK3C2A
0.925 0.040 11 17138601 intron variant A/G snv 0.31 3
rs1042779
ITIH1
0.882 0.040 3 52786995 missense variant A/G snv 0.40 0.42 2
rs10503253
CSMD1
0.851 0.040 8 4323322 intron variant C/A snv 0.18 2
rs10774037
CACNA1C
0.882 0.040 12 2311360 intron variant G/A snv 0.77 2
rs10994338
ANK3
0.882 0.040 10 60421370 intron variant G/A snv 7.5E-02 2
rs10994397
ANK3
0.851 0.040 10 60519366 intron variant C/T snv 9.5E-02 2
rs11789399
LOC105376249
0.882 0.040 9 118597008 intergenic variant G/A;C snv 2
rs12201676 0.925 0.040 6 89022382 regulatory region variant T/C snv 0.21 2
rs12966547
LOC105372125
0.827 0.040 18 55084786 intergenic variant G/A snv 0.39 2
rs17645023 1.000 0.040 17 66920916 intergenic variant A/T snv 0.22 2
rs17662626
LOC107985969
0.851 0.040 2 193119895 intergenic variant A/G snv 5.9E-02 2
rs17746001 0.925 0.040 4 179734472 intergenic variant C/T snv 5.3E-02 2
rs1975802
PLA2G15
1.000 0.040 16 68251944 intron variant A/C;G snv 2
rs2021722
TRIM26
0.851 0.040 6 30206354 intron variant C/A;T snv 0.24 2
rs2054399
KCNMB2-AS1 ; KCNMB2
0.925 0.040 3 178623794 intron variant G/A;C snv 2
rs2312147
VRK2
1.000 0.040 2 57995793 intron variant T/C snv 0.70 2
rs2535629
ITIH3
0.827 0.040 3 52799203 intron variant G/A;C snv 2
rs4309482
LOC105372125
0.925 0.040 18 55083238 intergenic variant A/G snv 0.39 2