Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 19
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 5
rs1410996
CFH
0.807 0.240 1 196727803 intron variant G/A snv 0.46 5
rs800292
CFH
0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 5
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 4
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 4
rs267734 0.925 0.120 1 150979001 upstream gene variant T/C snv 0.14 3
rs6136
SELP
0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 3
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 3
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 3
rs10911021
LOC105371642 ; LINC01344
0.807 0.160 1 182112825 intron variant C/T snv 0.36 2
rs17111503
PCSK9
0.925 0.160 1 55037775 upstream gene variant A/G snv 0.22 2
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 2
rs505151
PCSK9
0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 2
rs5068
NPPA ; NPPA-AS1 ; CLCN6
0.776 0.160 1 11845917 3 prime UTR variant A/G;T snv 2
rs59825600
LOC105376759 ; KAZN
1.000 0.040 1 14806568 intron variant G/A snv 0.11 2
rs6688849 1.000 0.040 1 47530532 intergenic variant A/C;G snv 2
rs10494366
LOC105371475 ; NOS1AP
0.851 0.200 1 162115895 intron variant G/T snv 0.54 1
rs17106184
FAF1
0.925 0.080 1 50444313 intron variant G/A snv 8.5E-02 1
rs1967017 0.882 0.160 1 145711421 upstream gene variant A/G snv 0.43 1
rs2275558
PBX1
0.882 0.200 1 164559883 missense variant G/A snv 0.30 0.19 1
rs3789678
AGT
1.000 0.040 1 230713736 intron variant C/T snv 0.15 1
rs5063
CLCN6 ; NPPA-AS1 ; NPPA
0.763 0.280 1 11847591 missense variant C/T snv 5.6E-02 5.3E-02 1