Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 11
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 11
rs3130380
HCG18 ; HCG17
0.807 0.280 6 30311353 intron variant G/A snv 6.6E-02 10
rs9261290
RNF39
0.807 0.280 6 30070870 3 prime UTR variant T/C;G snv 5.2E-02; 7.2E-06 10
rs12153855
TNXB
0.776 0.320 6 32107027 intron variant T/C snv 0.11 10
rs12198173
TNXB
0.827 0.240 6 32059031 intron variant G/A snv 0.10 9
rs2248462 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 8
rs10484554
LOC112267902 ; HLA-B
0.807 0.200 6 31306778 intron variant C/T snv 0.12 8
rs2247056
LOC112267902 ; HLA-B ; LINC02571
0.882 0.160 6 31297713 intron variant T/C snv 0.80 8
rs13199524
TNXB
0.807 0.240 6 32098988 intron variant C/T snv 8.4E-02 8
rs185819
TNXB
0.851 0.200 6 32082290 missense variant T/A;C;G snv 8.2E-06; 0.58; 4.1E-06 8
rs2269426
TNXB
0.807 0.280 6 32108722 intron variant G/A snv 0.35 8
rs2516448 0.827 0.120 6 31422633 intron variant T/C;G snv 7
rs2523535 0.851 0.200 6 31368473 intron variant A/G snv 0.32 7
rs2844511 0.807 0.200 6 31422007 intron variant A/G;T snv 7
rs12663103
GPSM3
0.851 0.240 6 32193547 intron variant T/C snv 6.1E-02 7
rs2395029
HCP5
0.790 0.320 6 31464003 non coding transcript exon variant T/G snv 2.7E-02 2.4E-02 7
rs6457374
HLA-B ; LOC112267902
0.851 0.200 6 31304484 intron variant C/T snv 0.81 7
rs2516509
MICB-DT
0.882 0.160 6 31482217 intron variant T/C snv 0.19 7
rs3815087
PSORS1C1
0.851 0.200 6 31125810 5 prime UTR variant G/A snv 0.25 7
rs9368699
SNHG32 ; SNORD48
0.851 0.200 6 31834764 non coding transcript exon variant T/C snv 3.2E-02 7
rs13394720 1.000 2 233593475 intergenic variant T/C snv 7.0E-02 6
rs13437082 1.000 6 31386783 upstream gene variant C/T snv 0.32 6
rs2516400 0.827 0.320 6 31513328 upstream gene variant G/A snv 0.32 6
rs2844513 0.925 0.120 6 31420437 intron variant G/A snv 0.53 6