Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10
rs12509595 1.000 0.080 4 80261400 intergenic variant T/C snv 0.23 10
rs140522
ODF3B
0.851 0.160 22 50532837 upstream gene variant T/A;C snv 10
rs17758695
BCL2
18 63253621 intron variant C/T snv 2.1E-02 10
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 10
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
rs218265 4 54542832 intergenic variant T/C snv 0.21 9
rs35979828
NFE2
12 54292096 intron variant C/T snv 5.0E-02 9
rs10224210
PRKAG2
1.000 0.040 7 151716108 intron variant T/C snv 0.21 8
rs17476364
HK1
10 69334748 intron variant T/C snv 6.4E-02 8
rs2075672
TFR2 ; ACTL6B
7 100642673 intron variant A/G snv 0.65 8
rs62435145 1.000 0.040 7 1246931 regulatory region variant G/T snv 0.51 8
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40 8
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 7
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 7
rs2070895
LIPC ; ALDH1A2
0.807 0.120 15 58431740 intron variant G/A snv 0.33 7
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv 7
rs6993770
ZFPM2 ; ZFPM2-AS1
0.925 0.080 8 105569300 intron variant A/T snv 0.31 7
rs760077
MTX1 ; THBS3
0.925 0.120 1 155208991 missense variant T/A snv 0.36 7
rs9376090
HBS1L
6 135090090 intron variant T/C snv 0.19 7
rs9895661
BCAS3
0.882 0.200 17 61379228 non coding transcript exon variant C/T snv 0.69 7
rs10758656
RCL1
9 4852599 intron variant A/G snv 0.19 6
rs11553699
TMEM120B ; RHOF
12 121779004 3 prime UTR variant A/G snv 9.4E-02 6
rs12968719
PTPN2
0.827 0.120 18 12879467 intron variant G/A snv 8.5E-02 6
rs13125101 4 80253438 TF binding site variant G/A snv 0.24 6