Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7173766 15 54711241 intergenic variant A/G snv 0.92 2
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 1
rs4799668
LOC105372058
18 32836937 intron variant A/G snv 0.88 2
rs1516725
ETV5 ; DGKG
0.925 0.120 3 186106215 intron variant T/C snv 0.86 3
rs939583 1.000 0.080 2 622531 intergenic variant C/T snv 0.85 2
rs6548238 0.882 0.200 2 634905 TF binding site variant T/C snv 0.85 4
rs2903492 2 624678 intergenic variant G/A snv 0.85 2
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 3
rs2030323
BDNF
0.925 0.080 11 27706992 intron variant A/C snv 0.83 3
rs10767664
BDNF
0.752 0.400 11 27704439 intron variant T/A snv 0.83 2
rs9816226
DGKG
1.000 0.080 3 186116710 intron variant A/T snv 0.82 3
rs308971
SYN2
3 12075120 intron variant G/A snv 0.82 2
rs4854344 1.000 0.080 2 638144 regulatory region variant G/T snv 0.82 4
rs10173167 2 646767 intergenic variant G/A snv 0.82 2
rs7561317 0.925 0.120 2 644953 intergenic variant A/G snv 0.81 4
rs10261878 7 25910925 intergenic variant A/C snv 0.80 2
rs2922763 8 75661476 intergenic variant G/T snv 0.77 2
rs1211166
NTRK2
9 84671077 intron variant G/A snv 0.77 2
rs4854348 2 647760 intergenic variant A/G snv 0.77 2
rs4854349 2 647861 intergenic variant T/C snv 0.77 2
rs10193244 2 647580 intergenic variant T/C snv 0.77 2
rs7570198 2 648198 intergenic variant C/T snv 0.76 2
rs255414
LOC107986418
5 63522073 intergenic variant G/A snv 0.76 2
rs2904880
CD19 ; RABEP2
1.000 0.040 16 28933075 missense variant C/G snv 0.72 0.76 2
rs5996074
SREBF2
22 41840333 intron variant G/A snv 0.74 3