Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10068807 5 55581157 intergenic variant A/G snv 0.70 1
rs10269139
GLI3
7 42108589 intron variant C/T snv 0.31 1
rs10433500
CADM2
3 85497648 intron variant G/A snv 0.51 1
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
rs1056513
PATJ
1 61914626 missense variant G/A;C snv 0.57; 8.0E-06 2
rs10917220 1 22356912 intergenic variant T/C snv 0.65 1
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 8
rs11001398
LRMDA
10 75461756 intron variant G/A;C snv 1
rs11014285
PRTFDC1
10 24889935 intron variant G/A snv 0.11 2
rs11030119
BDNF
11 27706555 intron variant G/A;T snv 2
rs1108548
LINC02869
1 218461445 intron variant A/G snv 0.40 1
rs11128264 3 72343159 intergenic variant C/T snv 0.55 1
rs111352324
FAF1
1 50755008 intron variant T/C snv 8.7E-02 1
rs11136336
PLEC
8 143933019 missense variant G/A snv 0.33 0.29 1
rs11160601 14 100720304 regulatory region variant C/G;T snv 1
rs11187838
PLCE1-AS1 ; PLCE1
10 94278929 non coding transcript exon variant G/A snv 0.44 3
rs11200607
PLEKHA1
10 122395110 intron variant C/G;T snv 1
rs11243202 6 7718832 intergenic variant T/C snv 0.39 1
rs113191842
FTO
16 53783406 intron variant G/A snv 9.4E-02 5
rs113422653
LOC105373258 ; LINC02774
1 243978778 intron variant G/A snv 3.8E-02 1
rs115179432
LTBP1
2 33123612 intron variant A/G snv 5.6E-02 2
rs11597119
SLF2
10 100914591 intron variant A/G snv 0.35 1
rs11855017
MAPKBP1
15 41803948 intron variant C/A snv 0.15 2
rs11874191 18 38584120 intergenic variant C/T snv 0.66 1
rs11944404 4 144749719 intron variant T/C snv 0.39 1