Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3197999
MST1 ; APEH
0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 6
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 6
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 5
rs2858331 0.827 0.240 6 32713500 upstream gene variant A/G snv 0.42 5
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 5
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 5
rs3763313
BTNL2
0.807 0.320 6 32408694 upstream gene variant A/C snv 0.21 5
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 5
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 5
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 5
rs174537
TMEM258 ; MYRF
0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 5
rs2298428
YDJC
0.807 0.240 22 21628603 missense variant C/T snv 0.27 0.18 5
rs1569723 0.851 0.280 20 46113425 upstream gene variant C/A snv 0.80 4
rs2836878 0.851 0.200 21 39093608 intergenic variant G/A snv 0.23 4
rs5000634 0.851 0.200 6 32695787 intergenic variant A/G snv 0.39 4
rs9286879 0.851 0.200 1 172893094 intron variant A/G snv 0.32 4
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 4
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs10947261
BTNL2 ; TSBP1-AS1
0.882 0.240 6 32405455 splice region variant G/T snv 0.11 4
rs2201841
C1orf141 ; IL23R
0.716 0.440 1 67228519 intron variant A/G;T snv 4
rs2301436
FGFR1OP
0.752 0.320 6 167024500 intron variant C/T snv 0.42 4
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46 4
rs4537545
IL6R
0.790 0.160 1 154446403 intron variant C/T snv 0.48 4