Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6882366
CAST ; LOC101929710
5 96528989 intron variant C/T snv 0.39 2
rs11951673
LOC101929710 ; CAST
5 96525308 non coding transcript exon variant C/T snv 0.39 2
rs1837269
LOC101929710
5 96523440 intron variant C/T snv 0.53 2
rs10476682
LOC101929710
5 96522554 intron variant A/G snv 0.38 2
rs2611742
LOC101929710
5 96520797 intron variant T/C snv 0.43 2
rs1026534
LOC101929710 ; LOC107986362
5 96519387 intron variant G/C snv 0.60 2
rs263349
LOC101929710 ; LOC107986362
5 96515920 intron variant T/A;G snv 2
rs261967
LOC101929710 ; LOC107986362
5 96514546 intron variant A/C snv 0.42 2
rs261966
LOC107986362 ; LOC101929710
5 96513883 intron variant T/C snv 0.42 2
rs3853212
LOC107986362 ; LOC101929710
5 96513644 intron variant C/T snv 0.37 2
rs6556926
LOC101929710 ; LOC107986362
5 96512909 intron variant T/A snv 0.38 2
rs261964
LOC107986362 ; LOC101929710
5 96512372 intron variant T/C snv 0.60 2
rs10077823
LOC101929710 ; LOC107986362
5 96510626 intron variant A/G snv 0.43 2
rs7737742
LOC107986362 ; LOC101929710
5 96509543 intron variant T/C snv 0.59 2
rs1555543 1 96479241 intergenic variant A/C snv 0.55 2
rs10993160 9 94306644 downstream gene variant A/G snv 4.2E-02 2
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 1
rs3822072
FAM13A
4 88820118 intron variant G/A;C snv 4
rs6893807
LINC00461
5 88669203 non coding transcript exon variant A/G snv 0.21 2
rs9936833 0.882 0.160 16 86369512 intergenic variant C/T snv 0.64 3
rs13078807
CADM2
0.925 0.120 3 85835000 intron variant A/G snv 0.15 3
rs4929949
STK33
1.000 0.080 11 8583046 intron variant T/C snv 0.46 2
rs1211166
NTRK2
9 84671077 intron variant G/A snv 0.77 2
rs10769908
STK33
11 8462542 intron variant C/T snv 0.55 3
rs10150332
NRXN3
14 79470621 intron variant T/C snv 0.26 3