Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs78487399
THADA
2 43582208 intron variant G/C snv 6.2E-02 5
rs12035735
LRRC8D
1 89839786 intron variant G/A snv 1.4E-03 4
rs13277237
CCDC26
8 129592317 intron variant G/A snv 0.53 4
rs1799852
TF
3 133756878 synonymous variant C/T snv 0.13 0.11 3
rs1991866
CCDC26
8 129611859 intron variant G/A;C snv 3
rs11969064 6 18104864 intergenic variant C/T snv 0.11 2
rs62037363
SH2B1 ; TUFM
16 28853721 intron variant T/C snv 0.34 2
rs9557207
UBAC2
13 99384164 intron variant A/G snv 0.17 2
rs1003342
HORMAD2
22 30174033 intron variant A/G snv 0.45 1
rs10061469 5 73222321 intron variant T/C snv 0.37 1
rs10142466 14 68805067 intergenic variant A/C;G;T snv 1
rs10521318 16 85977731 intron variant C/G;T snv 1
rs10896794
LPXN
11 58571651 intron variant T/C snv 0.19 1
rs10956252
LOC105375746
8 125523895 intron variant C/G;T snv 1
rs11187157 10 92742487 TF binding site variant T/C snv 0.40 1
rs11612508
DUSP16
12 12504579 intron variant A/G snv 0.22 1
rs11641016 16 85981275 intron variant C/G snv 0.18 1
rs11677953 2 218256940 non coding transcript exon variant G/A snv 0.36 1
rs11708026
LOC105376976
3 18700310 intron variant A/G snv 0.11 1
rs11768365
LOC101927325 ; GRID2IP
7 6505557 intron variant A/G snv 0.26 1
rs12199775
PHACTR2
6 143577757 intron variant A/G snv 4.8E-02 1
rs12318183
LOC107984526 ; IFNG-AS1
12 68110056 intron variant C/A snv 0.34 1
rs1250566
ZMIZ1
10 79286696 intron variant G/A snv 0.24 1
rs12585310 13 26954210 intergenic variant G/A snv 0.27 1
rs1297258
LOC101927745
21 15434390 intron variant C/T snv 0.44 1