Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2789588 6 72433995 intergenic variant A/C snv 0.26 1
rs2007044
CACNA1C
0.882 0.040 12 2235794 intron variant A/G snv 0.50 1
rs2239547
ITIH4
0.882 0.040 3 52821213 intron variant T/C snv 0.27 1
rs5174
LRP8
0.776 0.240 1 53247055 missense variant C/T snv 0.29 0.28 1
rs1039002
PDE10A
0.851 0.080 6 165741969 intron variant G/A;T snv 1
rs4583255
TAOK2
16 29977620 intron variant A/G snv 0.36 1
rs17512836
TCF4
0.925 0.040 18 55527730 intron variant T/C snv 2.2E-02 1
rs9960767
TCF4
0.925 0.040 18 55487771 intron variant A/C;G snv 1
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 1
rs1009080 1 29958713 intergenic variant G/A snv 0.54 2
rs10949808 7 156255955 intergenic variant T/G snv 0.45 2
rs12201676 0.925 0.040 6 89022382 regulatory region variant T/C snv 0.21 2
rs12527359 6 89018502 intergenic variant T/A snv 0.23 2
rs12807809 0.882 0.160 11 124736389 upstream gene variant T/C snv 0.20 2
rs17069122 6 108002555 downstream gene variant G/A snv 1.9E-02 2
rs17075286 3 43189231 intergenic variant C/G snv 5.9E-02 2
rs17645023 1.000 0.040 17 66920916 intergenic variant A/T snv 0.22 2
rs17746001 0.925 0.040 4 179734472 intergenic variant C/T snv 5.3E-02 2
rs1806864 9 87416754 regulatory region variant G/C snv 7.4E-02 2
rs2018368 11 10718819 intergenic variant C/G snv 0.59 2
rs2155907 11 98223945 intergenic variant C/T snv 0.38 2
rs2509843 11 98254676 intergenic variant A/C;G;T snv 2
rs2841307 6 100308811 intergenic variant C/T snv 0.20 2
rs4949526 1.000 0.040 1 29959372 intergenic variant T/C snv 0.54 2
rs4996815 13 105999312 intron variant G/T snv 0.61 2