Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9921222
AXIN1
0.925 0.120 16 325782 intron variant C/T snv 0.51 2
rs4870044
CCDC170
1.000 0.080 6 151580274 intron variant C/T snv 0.44 2
rs2450083
COLEC10
1.000 0.080 8 119051303 intron variant T/C snv 0.59 2
rs13245690
CPED1
7 121145010 intron variant A/G snv 0.32 2
rs2414098
CYP19A1 ; MIR4713HG
1.000 0.080 15 51245609 intron variant T/C snv 0.65 2
rs917727
FAM3C
7 121378525 intron variant C/A;T snv 0.33 2
rs10901216
FUBP3
9 130596504 intron variant G/A snv 0.28 2
rs7466269
FUBP3
9 130588697 intron variant A/G snv 0.33 2
rs2955382
GID4
17 18044396 intron variant C/T snv 0.43 2
rs4480845
HIC1
17 2055315 intron variant T/C snv 0.64 2
rs4980659
LINC01488
11 69484769 intron variant C/A;G snv 2
rs9533090
LINC02341
13 42377313 intron variant C/T snv 0.39 2
rs7277076
LOC105369301 ; CLDN14
1.000 0.080 21 36464675 intron variant T/C snv 0.52 2
rs118115924
LOC105369757
12 48985754 downstream gene variant G/A;T snv 2
rs3920498
LOC105376850
1.000 0.040 1 22166394 intergenic variant G/C snv 0.19 2
rs7521902
LOC105376850
1.000 0.040 1 22164231 intergenic variant C/A snv 0.22 2
rs1262476
LOC105377992
6 126665850 intron variant A/G;T snv 2
rs10037512
MEF2C-AS1
5 89058858 intron variant T/A;C snv 2
rs1366594
MEF2C-AS1
5 89080244 intron variant A/C snv 0.57 2
rs6894139
MEF2C-AS1
5 89031965 non coding transcript exon variant T/G snv 0.57 2
rs1595824
PLCL1
2 198009282 intron variant C/A;T snv 2
rs13469
POLDIP2
17 28349109 synonymous variant C/G;T snv 0.53 2
rs12284933
PPP6R3
11 68552021 intron variant G/A snv 0.23 2
rs505404
PSMD13
11 243268 non coding transcript exon variant T/G snv 0.28 2
rs73169678
SMARCD3
7 151256119 intron variant C/A;T snv 2