Source: GWASDB

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 13
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 9
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 8
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 8
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 8
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 7
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 7
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 6
rs3748816
MMEL1
0.827 0.200 1 2595307 missense variant A/G snv 0.41 0.46 6
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 6
rs2474937 0.851 0.120 1 118360355 intergenic variant A/G snv 0.25 6
rs4970834
CELSR2
0.925 0.160 1 109272258 intron variant C/T snv 0.17 0.21 6
rs5176
LRP8
1 53246137 3 prime UTR variant T/G snv 6.4E-04 6
rs583104 1 109278685 downstream gene variant G/T snv 0.63 6
rs370911
NOS1AP
1 162323515 intron variant A/G snv 0.99 6
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs2816316
LOC105371664
0.882 0.200 1 192567683 intron variant C/A snv 0.79 5
rs296547
MROH3P
0.882 0.200 1 200923009 intron variant T/C snv 0.53 5
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 5
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 5
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 5
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 5
rs2568958
LOC105378797
0.882 0.160 1 72299433 intron variant G/A;C snv 5
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5