Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17036328
PPARG
1.000 0.040 3 12348985 intron variant T/C snv 0.14 3
rs7544735
RNU6ATAC35P
1.000 0.040 1 220825571 intron variant G/A snv 0.22 3
rs7090135
RPS24
0.882 0.080 10 78043832 intron variant G/A;C snv 0.13 3
rs10054105
STARD4-AS1
0.925 0.080 5 111573636 intron variant T/G snv 0.17 3
rs8177248
TF
1.000 0.040 3 133760782 non coding transcript exon variant C/T snv 0.28 3
rs8177253
TF
1.000 0.040 3 133761348 non coding transcript exon variant C/T snv 0.31 3
rs41520844
WRN
0.882 0.080 8 31135670 intron variant A/T snv 7.1E-02 3
rs499459
WTAPP1
0.925 0.080 11 102822455 intron variant A/G snv 0.90 3
rs564018
WTAPP1
0.925 0.080 11 102820688 intron variant A/G;T snv 3
rs8088980
ZNF407
1.000 0.040 18 74666435 intron variant C/T snv 0.51 3
rs11264339 1.000 0.040 1 155168172 downstream gene variant C/T snv 0.56 2
rs2380205 0.882 0.080 10 5844771 upstream gene variant C/T snv 0.47 2
rs2452877 1.000 0.040 5 4027643 regulatory region variant A/G snv 0.60 2
rs2597513 1.000 0.040 3 13514336 regulatory region variant C/T snv 0.88 2
rs2726034 1.000 0.040 16 28325561 downstream gene variant T/C snv 0.37 2
rs3893384 1.000 0.040 15 79680713 regulatory region variant C/T snv 0.50 2
rs4307059 0.882 0.080 5 25967594 intron variant T/A;C snv 2
rs563697 1.000 0.040 2 118656877 intergenic variant A/G snv 0.25 2
rs7929543 0.925 0.120 11 49329474 intron variant A/C snv 0.12 2
rs2622629
ABCG2
0.882 0.160 4 88172912 intron variant T/C snv 0.28 2
rs13395354
ACOXL
1.000 0.040 2 110842942 intron variant C/T snv 0.18 2
rs7089424
ARID5B
0.752 0.200 10 61992400 intron variant T/G snv 0.32 2
rs6559921
C9orf153
1.000 0.040 9 86257124 intron variant A/T snv 0.26 2
rs3911063
CADM2
1.000 0.040 3 85857778 intron variant T/C snv 0.30 2
rs4938642
CBL
1.000 0.040 11 119229196 intron variant G/C snv 6.0E-02 2