Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3810291
ZC3H4
19 47065746 3 prime UTR variant G/A snv 0.50 7
rs2238732
PRODH
22 18927834 intron variant C/G;T snv 7
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs75885714
PLCL2
3 16901018 intron variant A/C snv 4.6E-02 7
rs115849089 8 20054859 intergenic variant G/A snv 9.8E-02 7
rs17035646
CASZ1
1 10736490 intron variant G/A;T snv 6
rs112259268 17 43797377 downstream gene variant C/A snv 1.9E-02 6
rs11099097 4 80246155 intergenic variant C/T snv 0.30 6
rs10255839
EVX1
7 27249498 intron variant G/A snv 0.87 6
rs2643826 3 27521497 upstream gene variant C/T snv 0.56 6
rs55872725
FTO
16 53775211 intron variant C/T snv 0.31 6
rs1290784
MECOM
3 169379112 intron variant C/A;T snv 6
rs62434129
PLEKHG1
6 150687701 intron variant A/G;T snv 8.8E-02 6
rs2575876
ABCA1
9 104903458 intron variant G/A snv 0.24 6
rs2642438
MTARC1
1 220796686 missense variant A/G snv 0.75 0.78 6
rs13125101 4 80253438 TF binding site variant G/A snv 0.24 6
rs72681869
SOS2
14 50188639 missense variant G/A;C snv 4.0E-06; 4.1E-03 6
rs17216707 20 54115823 intergenic variant T/C snv 0.17 6
rs1533988 7 1253374 intergenic variant A/T snv 0.59 6
rs10409243
S1PR2 ; DNMT1
19 10222312 3 prime UTR variant C/A;G;T snv 6
rs415895
SWAP70
11 9748015 missense variant C/G snv 0.62 0.61 6
rs1887320 20 10985350 intron variant G/A snv 0.46 6
rs9349205
CCND3
6 41957421 intron variant G/A;C snv 6
rs10758656
RCL1
9 4852599 intron variant A/G snv 0.19 6
rs737092 20 57415349 regulatory region variant T/C snv 0.58 6