Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 6
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 6
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 5
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 5
rs10871777 0.925 0.120 18 60184530 intergenic variant A/G snv 0.24 4
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 4
rs8089364 0.925 0.120 18 60191596 upstream gene variant T/C snv 0.21 4
rs12967135 18 60181790 intergenic variant G/A snv 0.24 3
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 3
rs11152213 1.000 0.080 18 60185715 intergenic variant A/C;T snv 2
rs12954782 1.000 0.080 18 60196859 non coding transcript exon variant C/G snv 0.22 2
rs12969709 1.000 0.080 18 60192330 upstream gene variant C/A snv 0.21 2
rs1457489 1.000 0.080 18 60194728 upstream gene variant G/A snv 0.29 2
rs476828 1.000 0.080 18 60185354 intergenic variant T/C snv 0.28 2
rs538656 1.000 0.080 18 60183189 intergenic variant G/T snv 0.27 2
rs921971 1.000 0.080 18 60194430 upstream gene variant T/C snv 0.21 2
rs2168711 18 60181298 intergenic variant T/C snv 0.24 1
rs489693 1.000 0.080 18 60215554 intergenic variant C/A;T snv 1
rs523288 18 60181136 intergenic variant A/T snv 0.27 1
rs7654585 4 25941129 intergenic variant A/G snv 0.60 1
rs127430
APCDD1L-DT
20 58589799 intron variant A/G;T snv 1
rs7601155
BABAM2
2 28124815 intron variant C/T snv 6.8E-02 1
rs6867983
C5orf67
5 56558326 intron variant C/T snv 0.17 1
rs1516725
ETV5 ; DGKG
0.925 0.120 3 186106215 intron variant T/C snv 0.86 3
rs7132908
FAIM2
1.000 0.080 12 49869365 3 prime UTR variant G/A snv 0.31 1